Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1165196
SLC17A1
0.882 0.200 6 25812922 missense variant G/A snv 0.62 0.66 4
rs1165209
SLC17A1
0.925 0.120 6 25801091 intron variant G/A snv 0.66 4
rs1165215
SLC17A1
0.882 0.200 6 25798704 3 prime UTR variant G/A snv 0.66 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
rs1185567
SLC17A1
0.925 0.120 6 25818360 intron variant A/G;T snv 4
rs1185569
SLC17A1
0.925 0.120 6 25831375 intron variant A/G snv 0.65 4
rs13197601
SLC17A1
0.882 0.200 6 25785707 intron variant G/A snv 0.32 4
rs2762353
SLC17A1
0.882 0.200 6 25794203 intron variant A/G snv 0.66 4
rs3757131
SLC17A1
0.882 0.200 6 25783681 intron variant C/T snv 0.32 4
rs3799344
SLC17A1
0.882 0.200 6 25786765 intron variant C/T snv 0.41 4
rs3799352
SLC17A1
0.925 0.120 6 25822392 intron variant C/T snv 0.65 4
rs765285
SLC17A1
0.925 0.120 6 25828014 intron variant G/C;T snv 4
rs11754288
SLC17A4 ; SLC17A1
0.925 0.120 6 25776721 missense variant G/A snv 0.36 0.32 4
rs10498730
SLC17A1
0.925 0.120 6 25811841 intron variant A/G snv 3.7E-02 3
rs13200784
SLC17A1
0.925 0.120 6 25829405 intron variant A/T snv 0.27 3
rs1324082
SLC17A1
0.925 0.120 6 25801743 intron variant C/T snv 0.28 3
rs1408268
SLC17A1
0.925 0.120 6 25826758 intron variant T/A snv 0.26 3
rs3799346
SLC17A1
0.882 0.200 6 25791126 intron variant C/T snv 0.28 3