ClinVar Miner

Submissions for variant NM_001204.7(BMPR2):c.1413+10A>T

gnomAD frequency: 0.00001  dbSNP: rs1388869180
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001424302 SCV001626898 likely benign Primary pulmonary hypertension 2018-03-10 criteria provided, single submitter clinical testing

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