List of variants reported as benign for Hypercholesterolemia, familial, 1 by Iberoamerican FH Network

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_174936.4(PCSK9):c.207+15A>G	rs2495482	0.91171
NM_174936.4(PCSK9):c.1380A>G (p.Val460=)	rs540796	0.82761
NM_174936.4(PCSK9):c.799+3A>G	rs2495477	0.49156
NM_174936.4(PCSK9):c.658-7C>T	rs2483205	0.45035
NM_000527.5(LDLR):c.940+36G>A	rs13306513	0.03637
NM_000384.3(APOB):c.3337G>C (p.Asp1113His)
NM_000527.5(LDLR):c.1359-30C>T
NM_000527.5(LDLR):c.2177C>T (p.Thr726Ile)
NM_174936.4(PCSK9):c.2009G>A (p.Gly670Glu)
NM_174936.4(PCSK9):c.45GCT[8] (p.Leu23dup)	rs35574083

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