ClinVar Miner

Submissions for variant NM_058246.4(DNAJB6):c.621-4A>G

dbSNP: rs927500992
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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) RCV000594049 SCV000706870 uncertain significance not provided 2017-03-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003767390 SCV004637688 likely benign Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) 2023-07-17 criteria provided, single submitter clinical testing

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