Source: GWASCAT

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 55
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 4
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 3
rs6547692
GCKR
1.000 0.080 2 27512105 intron variant G/A snv 0.58 2
rs814295
GCKR
0.925 0.120 2 27520348 intron variant A/G snv 0.18 2
rs780096
GCKR
2 27518205 intron variant C/A;G snv 1
rs149847328
GCKR
1.000 0.080 2 27503548 stop gained C/T snv 3.1E-04 1.0E-04 1
rs57634090
GCKR
2 27508873 intron variant T/-;TT;TTT;TTTT;TTTTTT delins 1
rs780095
GCKR
2 27518238 intron variant A/G snv 0.60 1
rs8179252
GCKR
0.882 0.120 2 27523965 downstream gene variant A/C snv 0.37 1
rs2293571
GCKR
0.882 0.120 2 27506613 non coding transcript exon variant G/A snv 0.40 0.39 1