ClinVar Miner

Submissions for variant NM_139343.3(BIN1):c.315+7A>C

dbSNP: rs1573647825
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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 RCV000982826 SCV001130845 likely benign Myopathy, centronuclear, 2 2019-03-19 criteria provided, single submitter clinical testing

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