ClinVar Miner

Submissions for variant GRCh38/hg38 3q11.2(chr3:97779512-97864516)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Advanced Center For Translational And Genetic Medicine, Ann & Robert H. Lurie Children's Hospital Of Chicago RCV000498722 SCV000296046 likely pathogenic Bardet-Biedl syndrome 2016-07-20 no assertion criteria provided research

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