List of variants reported as uncertain significance for autosomal recessive limb-girdle muscular dystrophy type 2C by Genome-Nilou Lab

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000231.3(SGCG):c.653T>C (p.Ile218Thr)	rs202045534	0.00011
NM_000231.3(SGCG):c.101G>A (p.Arg34His)	rs755404457	0.00005
NM_000231.3(SGCG):c.267A>G (p.Pro89=)	rs149595403	0.00001
NM_000231.3(SGCG):c.547C>T (p.Leu183Phe)	rs1425113474	0.00001
NM_000231.3(SGCG):c.740T>C (p.Leu247Pro)	rs2137534069

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