ClinVar Miner

Submissions for variant NM_030761.5(WNT4):c.951G>A (p.Thr317=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002894728 SCV003236737 likely benign not provided 2025-01-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005019421 SCV005643906 likely benign Mullerian aplasia and hyperandrogenism; SERKAL syndrome 2024-03-27 criteria provided, single submitter clinical testing

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