Disease: Serum total cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9