ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.1087C>T (p.Gln363Ter)

dbSNP: rs2059695805
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centogene AG - the Rare Disease Company RCV001250160 SCV001424403 pathogenic Duchenne muscular dystrophy criteria provided, single submitter clinical testing

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