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</style></div></div><main class="main-wrapper"><header class="section_header"><div class="padding-global"><div class="container-large"><div class="header_content"><div class="padding-section-large"><div class="max-width-medium"><div class="margin-bottom margin-small"><h1 class="heading-style-h2">Mastermind Genomic Intelligence Platform</h1></div><p class="text-color-white">The World of Genomic Literature at your Fingertips</p><div class="margin-top margin_medium"><img src="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/666afe74da93cf1d3950a694_MM_Land_Tag_White1.png" loading="lazy" sizes="(max-width: 479px) 100vw, 357.671875px" srcset="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/666afe74da93cf1d3950a694_MM_Land_Tag_White1-p-500.png 500w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/666afe74da93cf1d3950a694_MM_Land_Tag_White1-p-800.png 800w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/666afe74da93cf1d3950a694_MM_Land_Tag_White1-p-1080.png 1080w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/666afe74da93cf1d3950a694_MM_Land_Tag_White1-p-1600.png 1600w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/666afe74da93cf1d3950a694_MM_Land_Tag_White1.png 1775w" alt="" class="image-23"/><div class="margin-top margin_medium"><a href="https://mastermind.genomenon.com/users/sign_up/?ref=gweb_mmpage" target="_blank" class="outline-button-white w-inline-block"><div class="button-label---white">Get Started</div></a></div></div></div></div></div></div></div><div class="header_background-image-wrapper"><div class="image-overlay-layer"></div><img src="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/667b92218f98c8b7c33b48ff_Subtract%20(4).png" loading="eager" sizes="(max-width: 991px) 100vw, 50vw" srcset="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/667b92218f98c8b7c33b48ff_Subtract%20(4)-p-500.png 500w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/667b92218f98c8b7c33b48ff_Subtract%20(4)-p-800.png 800w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/667b92218f98c8b7c33b48ff_Subtract%20(4)-p-1080.png 1080w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/667b92218f98c8b7c33b48ff_Subtract%20(4)-p-1600.png 1600w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/667b92218f98c8b7c33b48ff_Subtract%20(4)-p-2000.png 2000w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/667b92218f98c8b7c33b48ff_Subtract%20(4)-p-2600.png 2600w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/667b92218f98c8b7c33b48ff_Subtract%20(4).png 2707w" alt="" class="header5_background-image"/></div></header><div class="padding-section-medium"><div class="margin-bottom margin-medium"><div class="text-align-center"><h2>Built for the Needs of Your Industry</h2></div></div><div data-current="Clinical" data-easing="ease" data-duration-in="300" data-duration-out="100" class="tabs w-tabs"><div class="tabs-generic w-tab-menu"><a data-w-tab="Clinical" class="tab clinical w-inline-block w-tab-link w--current"><div>Mastermind for Clinical Diagnostics</div></a><a data-w-tab="Pharma" class="tab pharma w-inline-block w-tab-link"><div>Mastermind for Precision Therapeutics</div></a></div><div class="w-tab-content"><div data-w-tab="Clinical" class="tab-panel---clinical w-tab-pane w--tab-active"><div class="tab-content"><div class="tab-content-full-width"><h4>Be confident you have all the information you need for variant interpretation</h4><p>A 2020 study* reported that laboratories disagreed on a variant’s classification 46% of the time, with 23% of those discrepancies being clinically impactful. Access to comprehensive evidence is critical for proper diagnosis.</p></div></div><div class="benefits"><div class="tile-3x3"><div class="icon"><div class="icon_image icon_color-cyan w-embed"><svg xmlns="http://www.w3.org/2000/svg" width="100%" height="100%" viewBox="0 0 24 24" style="fill: rgba(0, 0, 0, 1);transform: ;msFilter:;" preserveAspectRatio="xMidYMid meet" aria-hidden="true" role="img"><path d="M12 2C6.486 2 2 6.486 2 12s4.486 10 10 10 10-4.486 10-10S17.514 2 12 2zm0 18c-4.411 0-8-3.589-8-8s3.589-8 8-8 8 3.589 8 8-3.589 8-8 8z" fill="currentColor"/><path d="M13 7h-2v6h6v-2h-4z" fill="currentColor"/></svg></div></div><h4>Reduce Turnaround Time</h4><p>Explore our continually growing catalog of pre-classified variants, designed to facilitate the rapid uncovering and interpretation of novel genetic variations. <br/><br/>Access valuable gene and variant summary information to streamline your analysis and deepen your insights.</p></div><div class="tile-3x3"><div class="icon"><img loading="lazy" src="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/66141032b380d971eeef4a55_trending-up.svg" alt="" class="icon_image"/></div><h4>Increase Diagnostic Yield</h4><p>Gain confidence in identifying more disease-causing variants leveraging our Genomic Intelligence Platform. <br/><br/>Our genomic language processing technology empowers you to uncover more disease-causing variants with precision.</p></div><div class="tile-3x3"><div class="icon"><img loading="lazy" src="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/6614103239000d93c773e4af_accelerate.svg" alt="" class="icon_image"/></div><h4>Accelerate Throughput</h4><p>Optimize your workflows by rapidly prioritizing variants of disease-causing genes. <br/><br/>This efficient process reduces resources, simplifying your analysis and enabling a more targeted approach.</p></div></div></div><div data-w-tab="Pharma" class="tab-panel---pharma w-tab-pane"><div class="tab-content"><div class="tab-content-full-width"><h4><strong>The Mastermind Genomic Intelligence Platform</strong></h4><p>Mastermind<sup> </sup>gives you access to all the information that's available on your disease of interest already curated and ready to go. <br/><br/>You can search by variant, gene, disease, therapy, and more. Mastermind contains the full text of more than 9.5 million publications, which are easily searchable by gene, variant, disease, and other key terms.</p></div></div><div class="benefits"><div class="tile-3x3"><div class="icon"><div class="icon-embed-small icon-color-purple w-embed"><svg xmlns="http://www.w3.org/2000/svg" width="100%" height="100%" viewBox="0 0 24 24" style="fill: rgba(0, 0, 0, 1);transform: ;msFilter:;" preserveAspectRatio="xMidYMid meet" aria-hidden="true" role="img"><path d="M12 2C6.486 2 2 6.486 2 12s4.486 10 10 10 10-4.486 10-10S17.514 2 12 2zm0 18c-4.411 0-8-3.589-8-8s3.589-8 8-8 8 3.589 8 8-3.589 8-8 8z" fill="currentColor"/><path d="M13 7h-2v6h6v-2h-4z" fill="currentColor"/></svg></div></div><h4><strong>Save Time and Minimize Expenses</strong></h4><p>Expedite your research workflow with instant access to the entirety of genomic research, pre-annotated by gene, variant, disease, and therapeutic.</p></div><div class="tile-3x3"><div class="icon"><div class="icon-embed-small icon-color-purple w-embed"><svg xmlns="http://www.w3.org/2000/svg" width="100%" height="100%" viewBox="0 0 24 24" style="fill: rgba(0, 0, 0, 1);transform: ;msFilter:;"><path d="m10 10.414 4 4 5.707-5.707L22 11V5h-6l2.293 2.293L14 11.586l-4-4-7.707 7.707 1.414 1.414z" fill="currentcolor"></path></svg></div></div><h4><strong>Accelerate Trial Eligibility Decisions</strong></h4><p>Get the information you need to make an educated decision faster through an easy-to-use search interface that returns prioritized, filterable literature results for identified variants.</p></div><div class="tile-3x3"><div class="icon"><div class="icon-embed-small icon-color-purple w-embed"><svg xmlns="http://www.w3.org/2000/svg" width="100%" height="100%" viewBox="0 0 24 24" style="fill: rgba(0, 0, 0, 1);transform: ;msFilter:;"><path d="M19.023 16.977a35.13 35.13 0 0 1-1.367-1.384c-.372-.378-.596-.653-.596-.653l-2.8-1.337A6.962 6.962 0 0 0 16 9c0-3.859-3.14-7-7-7S2 5.141 2 9s3.14 7 7 7c1.763 0 3.37-.66 4.603-1.739l1.337 2.8s.275.224.653.596c.387.363.896.854 1.384 1.367l1.358 1.392.604.646 2.121-2.121-.646-.604c-.379-.372-.885-.866-1.391-1.36zM9 14c-2.757 0-5-2.243-5-5s2.243-5 5-5 5 2.243 5 5-2.243 5-5 5z" fill="currentcolor"></path></svg></div></div><h4><strong>Characterize and Prioritize Targets and Programs</strong></h4><p>Accelerate research on potential targets and programs through prioritized and filterable literature results for the gene and/or disease of interest.</p></div></div></div></div></div><div class="padding-global"><div class="container-large"><div class="padding-section-large"><div class="w-layout-grid cta51_component"><div class="cta51_card"><div class="text-align-center"><div><div class="margin-bottom margin-small"><h2 class="text-color-white">Thousands of labs are using Mastermind to increase diagnostic yield.</h2></div><p class="text-color-white">Start searching the world's most comprehensive source of genomic evidence. Create your free account today.</p></div></div><div class="margin-top margin-medium"><div class="button-group is-center"><a href="https://mastermind.genomenon.com/users/sign_up/?ref=gweb_mmpage" class="button-filled---blue w-inline-block"><div class="button-label---white">Get started</div></a></div></div></div></div></div></div></div></div><div class="section_features"><div class="section_features"><div class="padding-global"><div class="container-medium"><div class="padding-section-medium"><div class="margin-bottom margin-medium"><div class="text-align-center"><h2>Features</h2></div></div><div class="feature_component padding-medium background-color-light-blue"><div class="w-layout-grid _1-col-grid"><div class="w-layout-grid layout1_component"><div class="layout1_image-wrapper"><img src="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6754481c4fc2dc89506f_Mastermind%20Gene%20Profile%20Page%20BRCA2%20breast%20cancer%20results.png" loading="lazy" sizes="(max-width: 479px) 87vw, (max-width: 767px) 83vw, 40vw" srcset="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6754481c4fc2dc89506f_Mastermind%20Gene%20Profile%20Page%20BRCA2%20breast%20cancer%20results-p-500.png 500w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6754481c4fc2dc89506f_Mastermind%20Gene%20Profile%20Page%20BRCA2%20breast%20cancer%20results-p-800.png 800w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6754481c4fc2dc89506f_Mastermind%20Gene%20Profile%20Page%20BRCA2%20breast%20cancer%20results-p-1080.png 1080w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6754481c4fc2dc89506f_Mastermind%20Gene%20Profile%20Page%20BRCA2%20breast%20cancer%20results-p-1600.png 1600w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6754481c4fc2dc89506f_Mastermind%20Gene%20Profile%20Page%20BRCA2%20breast%20cancer%20results-p-2000.png 2000w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6754481c4fc2dc89506f_Mastermind%20Gene%20Profile%20Page%20BRCA2%20breast%20cancer%20results-p-2600.png 2600w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6754481c4fc2dc89506f_Mastermind%20Gene%20Profile%20Page%20BRCA2%20breast%20cancer%20results.png 3140w" alt="" class="layout1_image"/></div><div class="layout1_content"><div class="margin-bottom margin-small"><h2>Gene Profile Page</h2></div><p>The Gene page allows users to access essential information from a variety of sources like ClinVar, ClinGen, DECIPHER, and gnomAD. Researchers can enhance their productivity by accessing details about {manually curated} gene-disease relationships, variant types, pathogenicity, and gene summaries all in one place.<br/><br/>From the gene page, users can seamlessly go to article searches and access data from Genomenon’s curated content and public sources like ClinVar.</p></div></div><div id="w-node-fadf313b-b1e2-bcef-7e2a-bb41b2b30d47-1b2f6144" class="w-layout-grid layout1_component"><div class="layout1_content"><div class="margin-bottom margin-small"><h2>Variant Evidence Page</h2></div><p>Discover our enhanced Evidence page designed to streamline information, allowing users to efficiently prioritize, navigate, and explore insights on search parameters of interest. <br/><br/>Mastermind makes it easy by including sentence fragments where the search terms were found in the article. With improved speed and workflow, researchers can effortlessly access and search through articles and curated content.</p></div><div class="layout1_image-wrapper"><img src="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2.png" loading="lazy" sizes="(max-width: 479px) 100vw, (max-width: 767px) 83vw, 40vw" srcset="https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2-p-500.png 500w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2-p-800.png 800w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2-p-1080.png 1080w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2-p-1600.png 1600w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2-p-2000.png 2000w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2-p-2600.png 2600w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2-p-3200.png 3200w, https://cdn.prod.website-files.com/65fc70a01e6c219100ad94c4/673f6767b90bcce7bdca999c_Mastermind%20Variant%20Evidence%20Page%20BRCA2.png 3500w" alt="" class="layout1_image"/></div></div></div></div></div></div></div><section class="section_ckb"></section></div><div class="padding-global"></div></div><section class="section_faq"><div class="padding-global"><div class="container-large"><div class="padding-section-large"><div class="w-layout-grid cta51_component"><div class="cta51_card"><div class="text-align-center"><div class="max-width-large"><div class="margin-bottom margin-small"><h2 class="text-color-white">FAQ</h2></div><p class="text-color-white">Find answers to all of your pressing Mastermind questions here.</p></div></div><div class="margin-top margin-medium"><div class="button-group is-center"><a href="/faq" class="button button-secondary w-inline-block"><div>Learn more</div><div class="icon-embed-xsmall w-embed"><svg xmlns="http://www.w3.org/2000/svg" width="100%" height="100%" viewBox="0 0 24 24" style="fill: rgba(0, 0, 0, 1);transform: ;msFilter:;" preserveAspectRatio="xMidYMid meet" aria-hidden="true" role="img"><path d="m11.293 17.293 1.414 1.414L19.414 12l-6.707-6.707-1.414 1.414L15.586 11H6v2h9.586z" fill="currentcolor"/></svg></div></a></div></div></div></div></div></div></div></section><div class="section_features hide_mobile"><div class="padding-global"><div class="container-large"><div class="padding-section-medium"><div class="margin-bottom margin-medium"><div class="text-align-center"><h2>How Mastermind Compares</h2></div></div><div class="w-layout-blockcontainer compare-table w-container"><div class="table-row table-header"><div class="compare-column-1"></div><div class="compare-column-2 callout-top"><div class="table-content-item bold">Mastermind</div></div><div class="compare-column-2"><div class="table-content-item">HGMD</div></div><div class="compare-column-2"><div class="table-content-item">ClinVar</div></div></div><div class="table-row"><div class="compare-column-1"><div class="table-content-item">Genes</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">19,353</div></div><div class="compare-column-2"><div class="table-content-item">18,959</div></div><div class="compare-column-2"><div class="table-content-item">17,548</div></div></div><div class="table-row alt-row"><div class="compare-column-1"><div class="table-content-item">Variants</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">26,651,819</div></div><div class="compare-column-2"><div class="table-content-item">535,428</div></div><div class="compare-column-2"><div class="table-content-item">2,322,570</div></div></div><div class="table-row"><div class="compare-column-1"><div class="table-content-item">Germline Variants</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">Yes</div></div><div class="compare-column-2"><div class="table-content-item">Yes</div></div><div class="compare-column-2"><div class="table-content-item">Yes</div></div></div><div class="table-row alt-row"><div class="compare-column-1"><div class="table-content-item">Somatic Variants</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">Yes</div></div><div class="compare-column-2"><div class="table-content-item">No</div></div><div class="compare-column-2"><div class="table-content-item">Yes</div></div></div><div class="table-row"><div class="compare-column-1"><div class="table-content-item">Journals</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">37,127</div></div><div class="compare-column-2"><div class="table-content-item">3,100</div></div><div class="compare-column-2"><div class="table-content-item">4,176</div></div></div><div class="table-row alt-row"><div class="compare-column-1"><div class="table-content-item">Full-Text Articles Indexed</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">10,255,990</div></div><div class="compare-column-2"><div class="table-content-item">72,987</div></div><div class="compare-column-2"><div class="table-content-item">121,862</div></div></div><div class="table-row"><div class="compare-column-1"><div class="table-content-item">Supplemental Datasets Indexed</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">3,652,377</div></div><div class="compare-column-2"><div class="table-content-item">N/A</div></div><div class="compare-column-2"><div class="table-content-item">N/A</div></div></div><div class="table-row alt-row"><div class="compare-column-1"><div class="table-content-item">Update Schedule</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">Weekly</div></div><div class="compare-column-2"><div class="table-content-item">Quarterly</div></div><div class="compare-column-2"><div class="table-content-item">Weekly</div></div></div><div class="table-row"><div class="compare-column-1"><div class="table-content-item">Free Version Content</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">Up to Date</div></div><div class="compare-column-2"><div class="table-content-item">3 Years Old</div></div><div class="compare-column-2"><div class="table-content-item">Up to Date</div></div></div><div class="table-row alt-row"><div class="compare-column-1"><div class="table-content-item">Interpretation Criteria</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">ACMG/AMP</div></div><div class="compare-column-2"><div class="table-content-item">Own Criteria</div></div><div class="compare-column-2"><div class="table-content-item">ACMG/AMP</div></div></div><div class="table-row"><div class="compare-column-1"><div class="table-content-item">ACMG Gene Curation Parameters</div></div><div class="compare-column-2 callout-middle"><div class="table-content-item">Yes</div></div><div class="compare-column-2"><div class="table-content-item">No</div></div><div class="compare-column-2"><div class="table-content-item">No</div></div></div><div class="table-row alt-row"><div class="compare-column-1"><div class="table-content-item">Clinical Exome Genes Curated based on ClinGen recommendations</div></div><div class="compare-column-2 callout-bottom"><div class="table-content-item">Yes</div></div><div class="compare-column-2"><div class="table-content-item">No</div></div><div class="compare-column-2"><div class="table-content-item">No</div></div></div></div></div></div></div></div><section class="section_pricing"><div class="padding-global"><div class="container-large"><div class="padding-section-large"><div class="margin-bottom margin-medium"><div class="text-align-center"><div class="max-width-large align-center"><div class="margin-bottom margin-small"><h2>Mastermind Plans</h2></div></div></div></div><div class="w-layout-grid pricing_plans"><div class="pricing_plan"><div class="pricing_content"><div class="pricing_content-top"><div class="margin-bottom margin-xsmall"><div class="heading-style-h3">Basic</div></div><div class="margin-bottom margin-medium"><div class="text-weight-medium">Free for Genomics Research</div></div><div class="pricing_feature-list"><div id="w-node-d7b70562-aa26-aa94-e16d-afd44e982b49-1b2f6144" class="pricing_feature"><div class="pricing_icon-wrapper"><div class="icon-embed-xsmall w-embed"><svg width="100%" height="100%" viewBox="0 0 24 24" fill="none" xmlns="http://www.w3.org/2000/svg">
<path d="M20.3479 7.56384L9.7479 18.1638C9.65402 18.2585 9.52622 18.3117 9.3929 18.3117C9.25958 18.3117 9.13178 18.2585 9.0379 18.1638L3.6479 12.7738C3.55324 12.68 3.5 12.5522 3.5 12.4188C3.5 12.2855 3.55324 12.1577 3.6479 12.0638L4.3479 11.3638C4.44178 11.2692 4.56958 11.2159 4.7029 11.2159C4.83622 11.2159 4.96402 11.2692 5.0579 11.3638L9.3879 15.6938L18.9379 6.14384C19.1357 5.95205 19.4501 5.95205 19.6479 6.14384L20.3479 6.85384C20.4426 6.94772 20.4958 7.07552 20.4958 7.20884C20.4958 7.34216 20.4426 7.46995 20.3479 7.56384Z" fill="currentColor"/>
</svg></div></div><div>Search 30M+ papers by gene and/or variant</div></div><div id="w-node-d7b70562-aa26-aa94-e16d-afd44e982b4e-1b2f6144" class="pricing_feature"><div class="pricing_icon-wrapper"><div class="icon-embed-xsmall w-embed"><svg width="100%" height="100%" viewBox="0 0 24 24" fill="none" xmlns="http://www.w3.org/2000/svg">
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</svg></div></div><div>Access causative association between genes and diseases</div></div><div id="w-node-ec05f8e0-595b-21a8-49ca-3704d781b5b0-1b2f6144" class="pricing_feature"><div class="pricing_icon-wrapper"><div class="icon-embed-xsmall w-embed"><svg width="100%" height="100%" viewBox="0 0 24 24" fill="none" xmlns="http://www.w3.org/2000/svg">
<path d="M20.3479 7.56384L9.7479 18.1638C9.65402 18.2585 9.52622 18.3117 9.3929 18.3117C9.25958 18.3117 9.13178 18.2585 9.0379 18.1638L3.6479 12.7738C3.55324 12.68 3.5 12.5522 3.5 12.4188C3.5 12.2855 3.55324 12.1577 3.6479 12.0638L4.3479 11.3638C4.44178 11.2692 4.56958 11.2159 4.7029 11.2159C4.83622 11.2159 4.96402 11.2692 5.0579 11.3638L9.3879 15.6938L18.9379 6.14384C19.1357 5.95205 19.4501 5.95205 19.6479 6.14384L20.3479 6.85384C20.4426 6.94772 20.4958 7.07552 20.4958 7.20884C20.4958 7.34216 20.4426 7.46995 20.3479 7.56384Z" fill="currentColor"/>
</svg></div></div><div>Get variant level curated insights, following ACMG guidelines</div></div><div id="w-node-ec05f8e0-595b-21a8-49ca-3704d781b5b5-1b2f6144" class="pricing_feature"><div class="pricing_icon-wrapper"><div class="icon-embed-xsmall w-embed"><svg width="100%" height="100%" viewBox="0 0 24 24" fill="none" xmlns="http://www.w3.org/2000/svg">
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</svg></div></div><div>Automated, real-time updates on highly sensitive data for every published variant</div></div><div id="w-node-ec05f8e0-595b-21a8-49ca-3704d781b5ba-1b2f6144" class="pricing_feature"><div class="pricing_icon-wrapper"><div class="icon-embed-xsmall w-embed"><svg width="100%" height="100%" viewBox="0 0 24 24" fill="none" xmlns="http://www.w3.org/2000/svg">
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