ClinVar Miner

Submissions for variant NM_025132.4(WDR19):c.1034T>G (p.Val345Gly)

dbSNP: rs387906983
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023684 SCV000044975 pathogenic Nephronophthisis 13 2011-11-11 no assertion criteria provided literature only

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