Disease: Serum total cholesterol measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs492602
LOC105447645 ; FUT2
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 6