ClinVar Miner

Submissions for variant NM_031372.4(HNRNPDL):c.92GGCCGC[3] (p.31RP[3])

dbSNP: rs1447722708
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001327101 SCV001518162 likely benign Autosomal dominant limb-girdle muscular dystrophy type 1G 2025-01-07 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001327101 SCV003808723 uncertain significance Autosomal dominant limb-girdle muscular dystrophy type 1G 2019-11-05 criteria provided, single submitter clinical testing

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