ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.6762+1G>A

dbSNP: rs886039534
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001937222 SCV002131886 pathogenic Duchenne muscular dystrophy 2021-08-12 criteria provided, single submitter clinical testing

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