ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.2853+1G>A

dbSNP: rs2151812559
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001726978 SCV001961560 pathogenic not provided 2021-09-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002477903 SCV002788023 pathogenic Polycystic kidney disease, adult type 2021-11-19 criteria provided, single submitter clinical testing

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