ClinVar Miner

Submissions for variant GRCh37/hg19 6p12.3-12.2(chr6:51695623-52371918)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Molecular and Human Genetics, Baylor College of Medicine RCV001195156 SCV001334116 pathogenic Autosomal recessive polycystic kidney disease 2020-04-16 no assertion criteria provided clinical testing

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