ClinVar Miner

Submissions for variant GRCh38/hg38 15q24.1(chr15:72714243-72720447)

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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 RCV000497631 SCV000296050 likely pathogenic Bardet-Biedl syndrome 2016-07-20 no assertion criteria provided research

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