ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.1704+20C>T

gnomAD frequency: 0.00003  dbSNP: rs762285101
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704350 SCV000528545 likely benign not provided 2018-11-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002059697 SCV002380794 likely benign Duchenne muscular dystrophy 2024-11-19 criteria provided, single submitter clinical testing

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