ClinVar Miner

Submissions for variant NM_058246.4(DNAJB6):c.63G>A (p.Lys21=)

dbSNP: rs886042682
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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) RCV000396152 SCV000335939 uncertain significance not provided 2015-10-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001471744 SCV001675860 likely benign Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) 2023-10-17 criteria provided, single submitter clinical testing

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