Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13015714
IL18R1
0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 1
rs1468788
SLC9A4
1.000 0.080 2 102476054 intron variant C/T snv 0.54 1
rs6498114
CIITA ; LOC105371080
1.000 0.080 16 10870261 intron variant G/T snv 0.78 1
rs7104791 1.000 0.080 11 111326133 downstream gene variant T/A;C snv 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 4
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs10886159 1.000 0.080 10 117854099 intergenic variant T/C snv 0.25 1
rs10892258
LOC105369519
0.925 0.120 11 118709156 intron variant G/A snv 0.19 4
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs61579022
ARHGAP31
1.000 0.080 3 119404431 intron variant G/A snv 0.30 1
rs1997179 1.000 0.080 4 122063478 intergenic variant T/C snv 0.21 1
rs13132933 0.925 0.200 4 122089432 upstream gene variant T/C snv 0.22 1
rs11938795
KIAA1109
0.882 0.120 4 122151854 upstream gene variant T/C snv 0.24 1
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs11734090
KIAA1109
1.000 0.080 4 122306958 intron variant T/C snv 0.25 1
rs6851362
KIAA1109
1.000 0.080 4 122342291 intron variant T/C snv 0.25 1
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 2