ClinVar Miner

Submissions for variant NM_058246.4(DNAJB6):c.678C>T (p.Ser226=)

dbSNP: rs768446425
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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 RCV002210764 SCV002492075 likely benign Autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6) 2023-12-14 criteria provided, single submitter clinical testing

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