ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.4674+9A>G

dbSNP: rs2147556976
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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 RCV001425086 SCV001627697 likely benign Duchenne muscular dystrophy 2020-10-30 criteria provided, single submitter clinical testing

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