ClinVar Miner

Submissions for variant NM_001202.6(BMP4):c.654C>T (p.Ser218=)

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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 RCV005005651 SCV005629336 uncertain significance Microphthalmia with brain and digit anomalies; Orofacial cleft 11 2024-02-13 criteria provided, single submitter clinical testing

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