ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.11537+2T>A

dbSNP: rs2151697557
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV001536123 SCV001752840 likely pathogenic Polycystic kidney disease, adult type 2021-06-30 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001536123 SCV002024639 likely pathogenic Polycystic kidney disease, adult type 2021-07-27 criteria provided, single submitter clinical testing

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