ClinVar Miner

List of variants reported as likely pathogenic for autosomal recessive limb-girdle muscular dystrophy type 2G by Evolutionary and Medical Genetics Laboratory,Center for Cellular and Molecular Biology

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_003673.3(TCAP):c.32C>A (p.Ser11Ter) rs45495192

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