ClinVar Miner

Submissions for variant NM_058246.4(DNAJB6):c.176-10C>A

dbSNP: rs764929861
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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 RCV001040202 SCV001203763 likely benign Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) 2024-11-19 criteria provided, single submitter clinical testing

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