ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.4344+39T>A

gnomAD frequency: 0.00149  dbSNP: rs72468644
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001718536 SCV001944139 benign not provided 2019-12-07 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832864 SCV002085334 likely benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2019-06-27 no assertion criteria provided clinical testing

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