ClinVar Miner

Submissions for variant NM_030761.5(WNT4):c.80A>G (p.Tyr27Cys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005015544 SCV005646971 uncertain significance Mullerian aplasia and hyperandrogenism; SERKAL syndrome 2024-05-13 criteria provided, single submitter clinical testing

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