ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.7065+21G>A

gnomAD frequency: 0.00418  dbSNP: rs9930234
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001304 SCV001158484 benign Polycystic kidney disease, adult type 2019-05-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001001304 SCV002795354 benign Polycystic kidney disease, adult type 2021-07-08 criteria provided, single submitter clinical testing

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