List of variants reported as uncertain significance for autosomal recessive limb-girdle muscular dystrophy type 2C by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000231.3(SGCG):c.157C>T (p.Leu53Phe)	rs138880406	0.00039
NM_000231.3(SGCG):c.596G>A (p.Arg199Gln)	rs200191311	0.00016
NM_000231.3(SGCG):c.653T>C (p.Ile218Thr)	rs202045534	0.00011
NM_000231.3(SGCG):c.142G>A (p.Val48Ile)	rs369936288	0.00008
NM_000231.3(SGCG):c.792C>G (p.Ile264Met)	rs377620885	0.00007
NM_000231.3(SGCG):c.436G>A (p.Asp146Asn)	rs373442790	0.00006
NM_000231.3(SGCG):c.1-3C>T	rs373335254	0.00005
NM_000231.3(SGCG):c.439G>A (p.Gly147Ser)	rs374836520	0.00004
NM_000231.3(SGCG):c.100C>T (p.Arg34Cys)	rs747549369	0.00001
NM_000231.3(SGCG):c.629A>G (p.His210Arg)	rs1045567625	0.00001
NM_000231.3(SGCG):c.781C>G (p.Leu261Val)	rs1460327315	0.00001

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