ClinVar Miner

Submissions for variant NM_006790.3(MYOT):c.634-15T>C

gnomAD frequency: 0.00082  dbSNP: rs115598221
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000250367 SCV000311592 benign not specified criteria provided, single submitter clinical testing
Invitae RCV002058215 SCV002462179 benign Myofibrillar myopathy 3 2023-12-27 criteria provided, single submitter clinical testing

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