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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000023.4(SGCA):c.*12+2T>C	rs1297436069	0.00001
NM_000023.4(SGCA):c.1064G>A (p.Arg355Gln)	rs1270625423	0.00001
NM_000023.4(SGCA):c.700G>A (p.Asp234Asn)	rs760608643	0.00001
NM_000023.4(SGCA):c.13C>G (p.Leu5Val)	rs2144488329
NM_000023.4(SGCA):c.541C>T (p.Arg181Cys)	rs574376340

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