ClinVar Miner

Submissions for variant NM_139343.3(BIN1):c.774+10G>A

gnomAD frequency: 0.00001  dbSNP: rs1684774289
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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 RCV002147107 SCV002413139 likely benign Myopathy, centronuclear, 2 2022-05-01 criteria provided, single submitter clinical testing

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