ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.497G>T (p.Gly166Val)

dbSNP: rs1557052538
Minimum review status: Collection method:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GenePathDx, GenePath diagnostics RCV000517210 SCV000616336 uncertain significance Duchenne muscular dystrophy 2017-06-07 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003144308 SCV003834778 uncertain significance not provided 2021-05-21 criteria provided, single submitter clinical testing

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