ClinVar Miner

Submissions for variant NM_006129.5(BMP1):c.962-37G>A

gnomAD frequency: 0.00114  dbSNP: rs78637678
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001567971 SCV001791754 likely benign not provided 2018-11-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001567971 SCV005222831 likely benign not provided criteria provided, single submitter not provided

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