ClinVar Miner

Submissions for variant NM_001202.6(BMP4):c.208C>T (p.Arg70Cys)

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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 RCV005007214 SCV005629352 uncertain significance Microphthalmia with brain and digit anomalies; Orofacial cleft 11 2024-05-24 criteria provided, single submitter clinical testing

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