ClinVar Miner

Submissions for variant NM_030761.5(WNT4):c.881G>A (p.Arg294His)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003148340 SCV003835106 uncertain significance Mullerian aplasia and hyperandrogenism 2021-12-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005021826 SCV005645823 uncertain significance Mullerian aplasia and hyperandrogenism; SERKAL syndrome 2024-05-08 criteria provided, single submitter clinical testing

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