606945.G

United Arab Emirates

Hypercholesterolemia

Unknown

Variant Name	Allele Count	Allele Frequency
NM_000527.4:c.1171G>A	2	0.025
NM_000527.4:c.81C>T	17	0.213
NM_000527.4:c.940+36G>A	6	0.075
NM_000527.4:c.1060+10G>C	36	0.45
NM_000527.4:c.1359-30C>T	38	0.475
NM_000527.4:c.1617C>T	3	0.038
NM_000527.4:c.1705+56C>T	10	0.125
NM_000527.4:c.1959T>C	38	0.475
NM_000527.4:c.2232A>G	59	0.738
NM_000527.4:c.2389+46C>T	16	0.2
NM_000527.4:c.*52G>A	13	0.163

11 benign polymorphisms identified in a group of patients with hypercholesterolemia. Polymorphisms may contribute to disease risk.