List of variants reported as likely benign for Hypercholesterolemia, familial, 1 by U4M - Lille University & CHRU Lille, Université de Lille - CHRU de Lille

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.1167G>A (p.Thr389=)	rs139066906	0.00052
NM_000527.5(LDLR):c.-28G>C	rs1131692188
NM_000527.5(LDLR):c.148G>T (p.Ala50Ser)	rs137853960
NM_000527.5(LDLR):c.1706-10G>A
NM_000527.5(LDLR):c.2231G>A (p.Arg744Gln)
NM_000527.5(LDLR):c.769C>T (p.Arg257Trp)
NM_000527.5(LDLR):c.829G>A (p.Glu277Lys)

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