List of variants reported as benign for Hypercholesterolemia, familial, 1 by All of Us Research Program, National Institutes of Health

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.1545C>T (p.Asn515=)	rs147896205	0.00183
NM_000527.5(LDLR):c.1887C>T (p.Phe629=)	rs751234870	0.00006
NM_000527.5(LDLR):c.993C>T (p.Asp331=)	rs147905921	0.00002
NM_000527.5(LDLR):c.1171G>A (p.Ala391Thr)

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