ClinVar Miner

Submissions for variant NM_001202.6(BMP4):c.-7-163C>G

dbSNP: rs10130587
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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 RCV001517844 SCV001726429 benign Microphthalmia with brain and digit anomalies; Orofacial cleft 11 2024-12-16 criteria provided, single submitter clinical testing
GeneDx RCV001597285 SCV001830953 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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