ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.10905A>G (p.Gln3635=)

dbSNP: rs1602138365
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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 RCV002093685 SCV002390634 likely benign Duchenne muscular dystrophy 2022-08-09 criteria provided, single submitter clinical testing

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