ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5064G>T (p.Val1688=)

dbSNP: rs886044345
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000403678 SCV000344592 uncertain significance not provided 2016-08-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001432892 SCV001635673 likely benign Duchenne muscular dystrophy 2025-01-06 criteria provided, single submitter clinical testing

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