ClinVar Miner

Submissions for variant NM_198334.3(GANAB):c.1541A>C (p.Asn514Thr)

dbSNP: rs1565094929
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Gastroenterology and Hepatology, Radboud University Medical Center RCV000758160 SCV000852186 uncertain significance Autosomal dominant polycystic kidney disease 2018-01-01 no assertion criteria provided research

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