List of variants reported as uncertain significance for Familial hypercholesterolemia by Laboratory of Molecular Genetics, National Medical Research Center for Therapy and Preventive Medicine

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.798T>A (p.Asp266Glu)	rs139043155	0.00004
NM_000527.5(LDLR):c.1784G>A (p.Arg595Gln)	rs201102492	0.00001
NM_000527.5(LDLR):c.2448G>C (p.Lys816Asn)	rs1399689294	0.00001
NM_000527.5(LDLR):c.1027G>A (p.Gly343Ser)
NM_000527.5(LDLR):c.1202T>A (p.Leu401His)	rs121908038
NM_000527.5(LDLR):c.1750T>C (p.Ser584Pro)	rs879255010
NM_000527.5(LDLR):c.1955T>C (p.Met652Thr)	rs875989936
NM_000527.5(LDLR):c.203G>T (p.Cys68Phe)	rs2077229853
NM_000527.5(LDLR):c.768C>A (p.Asp256Glu)	rs879254671
NM_000527.5(LDLR):c.829G>A (p.Glu277Lys)
NM_000527.5(LDLR):c.976T>C (p.Ser326Pro)	rs2077361498

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