ClinVar Miner

Submissions for variant NM_139343.3(BIN1):c.330G>C (p.Leu110=)

dbSNP: rs746946704
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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 RCV002196927 SCV002350662 likely benign Myopathy, centronuclear, 2 2021-10-23 criteria provided, single submitter clinical testing

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