Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1165160
SLC17A3
0.925 0.120 6 25864228 intron variant A/G snv 0.64 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
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
rs1185568
SLC17A3
0.925 0.120 6 25834200 intron variant T/A snv 0.65 4
rs6905614
SLC17A3
0.925 0.120 6 25840257 intron variant C/A;G snv 4
rs9393672
SLC17A3
0.925 0.120 6 25842377 intron variant T/G snv 0.51 4
rs942379
SLC17A3
0.925 0.120 6 25849392 missense variant A/G;T snv 0.60 4
rs1165148
SLC17A3
0.925 0.120 6 25844482 intron variant G/T snv 0.25 3
rs1165158
SLC17A3
0.925 0.120 6 25864670 intron variant C/A snv 0.25 3
rs1165159
SLC17A3
0.925 0.120 6 25864397 intron variant A/G snv 0.25 3
rs1165161
SLC17A3
0.925 0.120 6 25864134 intron variant C/T snv 0.25 3
rs1165162
SLC17A3
0.925 0.120 6 25863377 intron variant C/T snv 0.25 3
rs1165164
SLC17A3
0.925 0.120 6 25863253 intron variant G/A snv 0.24 3
rs1165165
SLC17A3
0.925 0.120 6 25862238 missense variant C/T snv 0.21 0.24 3
rs1165167
SLC17A3
0.925 0.120 6 25860460 intron variant A/G snv 0.25 3
rs1165187
SLC17A3
0.925 0.120 6 25851141 intron variant T/C snv 0.25 3
rs1165189
SLC17A3
0.925 0.120 6 25849551 intron variant A/C snv 0.25 3
rs1179087
SLC17A3
0.925 0.120 6 25858476 intron variant G/C;T snv 3
rs1182814
SLC17A3
0.925 0.120 6 25859326 intron variant T/C snv 0.25 3
rs1185978
SLC17A3
0.925 0.120 6 25835667 intron variant A/G snv 0.65 3
rs1408273
SLC17A3
0.925 0.120 6 25840718 intron variant A/G snv 0.51 3
rs1780969
SLC17A3
0.925 0.120 6 25858204 intron variant C/A snv 4.2E-03 3