ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5187A>G (p.Pro1729=)

dbSNP: rs1037540075
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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) RCV000730524 SCV000858267 uncertain significance not provided 2017-11-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001423338 SCV001625914 likely benign Duchenne muscular dystrophy 2022-11-09 criteria provided, single submitter clinical testing

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