ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.6915+27A>C

dbSNP: rs560681737
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001002104 SCV001159951 likely benign Polycystic kidney disease, adult type 2018-10-23 criteria provided, single submitter clinical testing

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