ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive limb-girdle muscular dystrophy type 2G; Hypertrophic cardiomyopathy 25 by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_003673.4(TCAP):c.469T>A (p.Ser157Thr)

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