List of variants reported as uncertain significance for Hypercholesterolemia, familial, 1 by Color Diagnostics, LLC DBA Color Health

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_174936.4(PCSK9):c.10G>A (p.Val4Ile)	rs186669805	0.00002
NM_000384.3(APOB):c.7283A>G (p.Lys2428Arg)	rs1369533953	0.00001
NM_174936.4(PCSK9):c.2023G>A (p.Val675Ile)	rs760981278	0.00001
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr)
NM_000384.3(APOB):c.3491G>A (p.Arg1164Lys)	rs759845943

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