ClinVar Miner

Submissions for variant NM_001161403.3(LIMS2):c.36C>T (p.Asn12=)

gnomAD frequency: 0.00067  dbSNP: rs150714487
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000254235 SCV000313121 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000544408 SCV000655773 likely benign Autosomal recessive limb-girdle muscular dystrophy type 2W 2024-11-28 criteria provided, single submitter clinical testing

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