ClinVar Miner

Submissions for variant NM_006790.3(MYOT):c.683+8del

dbSNP: rs760217241
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
Invitae RCV001080334 SCV000638821 likely benign Myofibrillar myopathy 3 2024-01-08 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000594296 SCV000705189 uncertain significance not provided 2018-04-04 criteria provided, single submitter clinical testing

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