ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.2853+23C>T

gnomAD frequency: 0.00520  dbSNP: rs183977076
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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 RCV001000289 SCV001156937 benign Polycystic kidney disease, adult type 2020-02-28 criteria provided, single submitter clinical testing

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