ClinVar Miner

List of variants reported as likely benign for Autosomal recessive limb-girdle muscular dystrophy type 2G; Hypertrophic cardiomyopathy 25

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_003673.3(TCAP):c.-13A>G	rs368175926	0.00010
NM_003673.4(TCAP):c.54G>C (p.Arg18=)	rs754054712	0.00004
NM_003673.4(TCAP):c.267G>A (p.Leu89=)	rs1419129039	0.00002

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