ClinVar Miner

Submissions for variant NM_139343.3(BIN1):c.1353C>G (p.Ala451=)

dbSNP: rs552244334
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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 RCV002136518 SCV002464584 likely benign Myopathy, centronuclear, 2 2020-10-30 criteria provided, single submitter clinical testing

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