ClinVar Miner

Submissions for variant NM_001202.6(BMP4):c.370+160C>T

dbSNP: rs2071047
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001517842 SCV001726427 benign Microphthalmia with brain and digit anomalies; Orofacial cleft 11 2023-10-13 criteria provided, single submitter clinical testing
GeneDx RCV001638112 SCV001852428 benign not provided 2018-06-26 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 27379672)

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