ClinVar Miner

Submissions for variant NM_058246.4(DNAJB6):c.479-10T>G

dbSNP: rs886042415
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000379729 SCV000334038 uncertain significance not provided 2015-09-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001500584 SCV001705376 likely benign Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) 2022-06-27 criteria provided, single submitter clinical testing

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