ClinVar Miner

Submissions for variant NM_139343.3(BIN1):c.630C>T (p.Ile210=)

dbSNP: rs886038728
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241976 SCV000315937 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000636921 SCV000758367 likely benign Myopathy, centronuclear, 2 2022-07-19 criteria provided, single submitter clinical testing

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