ClinVar Miner

Submissions for variant NM_139343.3(BIN1):c.698+19C>T

dbSNP: rs2105007728
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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 RCV002169912 SCV002338791 likely benign Myopathy, centronuclear, 2 2021-03-23 criteria provided, single submitter clinical testing

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