ClinVar Miner

Submissions for variant NM_139343.3(BIN1):c.213C>T (p.Ser71=)

dbSNP: rs560078675
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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 RCV000636913 SCV000758357 likely benign Myopathy, centronuclear, 2 2023-12-11 criteria provided, single submitter clinical testing

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