ClinVar Miner

Submissions for variant NM_004006.2(DMD):c.9352G>T (p.Ala3118Ser) (rs200928985)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics,Fulgent Genetics RCV000764876 SCV000896032 uncertain significance Becker muscular dystrophy; Duchenne muscular dystrophy; Dilated cardiomyopathy 3B 2018-10-31 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV000624887 SCV000740566 uncertain significance Familial dilated cardiomyopathy 2017-07-18 criteria provided, single submitter clinical testing

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