ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3900G>A (p.Glu1300=)

dbSNP: rs2148221514
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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 RCV001494453 SCV001699111 likely benign Duchenne muscular dystrophy 2021-08-24 criteria provided, single submitter clinical testing

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