ClinVar Miner

Submissions for variant NM_030761.5(WNT4):c.944T>G (p.Phe315Cys)

dbSNP: rs1334778982
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000714698 SCV000845420 uncertain significance SERKAL syndrome 2018-08-07 criteria provided, single submitter clinical testing
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000714699 SCV000845421 uncertain significance Mullerian aplasia and hyperandrogenism 2018-08-07 criteria provided, single submitter clinical testing
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000714700 SCV000845422 uncertain significance Mayer-Rokitansky-Kuster-Hauser syndrome 2018-08-07 criteria provided, single submitter clinical testing

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