ClinVar Miner

Submissions for variant NM_001161403.3(LIMS2):c.661-4G>C

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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 RCV002586213 SCV002932137 likely benign Autosomal recessive limb-girdle muscular dystrophy type 2W 2023-06-20 criteria provided, single submitter clinical testing

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