Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6976930
BAZ1B
0.925 0.120 7 73471480 intron variant G/A snv 0.23 5
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 5
rs7811265
BAZ1B
0.925 0.120 7 73520180 intron variant A/G snv 0.23 5
rs814295
GCKR
0.925 0.120 2 27520348 intron variant A/G snv 0.18 5
rs1028318
CARMIL1
0.925 0.120 6 25589996 intron variant T/C snv 0.27 4
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 4
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs10946785
CARMIL1
0.925 0.120 6 25616840 intron variant G/A;T snv 4
rs1165151
SLC17A1
0.925 0.120 6 25821388 intron variant T/A;G snv 4
rs1165152
SLC17A1
0.925 0.120 6 25818538 intron variant A/C;G;T snv 4
rs1165153
SLC17A1
0.925 0.120 6 25817561 intron variant A/G;T snv 4
rs1165160
SLC17A3
0.925 0.120 6 25864228 intron variant A/G snv 0.64 4
rs1165176
SLC17A1
0.925 0.120 6 25830070 intron variant A/G snv 0.65 4
rs1165177
SLC17A1
0.925 0.120 6 25829431 intron variant T/A snv 0.65 4
rs1165178
SLC17A1
0.925 0.120 6 25827288 intron variant A/G snv 0.65 4
rs1165182
SLC17A3
0.925 0.120 6 25837601 intron variant A/G snv 0.65 4
rs1165205
SLC17A3
0.925 0.120 6 25870314 intron variant T/A;G snv 4
rs1165207
SLC17A3
0.925 0.120 6 25865038 intron variant T/C snv 0.64 4
rs1165209
SLC17A1
0.925 0.120 6 25801091 intron variant G/A snv 0.66 4
rs11722228
SLC2A9
0.851 0.160 4 9914117 intron variant C/T snv 0.32 4
rs1183200
SLC17A1
0.925 0.120 6 25818418 intron variant G/C snv 0.66 4
rs1183201
SLC17A1
0.925 0.120 6 25823216 intron variant A/T snv 0.65 4
rs1184803
SLC17A3
0.925 0.120 6 25834430 intron variant T/C snv 0.65 4
rs1184804
SLC17A3
0.925 0.120 6 25867998 intron variant T/A;C snv 4
rs1185567
SLC17A1
0.925 0.120 6 25818360 intron variant A/G;T snv 4