ClinVar Miner

Submissions for variant NM_058246.4(DNAJB6):c.898+17A>G

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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 RCV002613874 SCV002961388 likely benign Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) 2022-06-26 criteria provided, single submitter clinical testing

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