ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.7065+1G>A

dbSNP: rs2151783532
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centogene AG - the Rare Disease Company RCV001808964 SCV002059264 likely pathogenic Polycystic kidney disease, adult type 2019-10-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001808964 SCV002797849 pathogenic Polycystic kidney disease, adult type 2022-04-10 criteria provided, single submitter clinical testing

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