Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051738
PDE4A
1.000 0.040 19 10467167 missense variant C/A;T snv 0.17; 4.8E-05 1
rs10782001
FBXL19
1.000 0.040 16 30931304 intron variant G/A snv 0.53 1
rs10794648 1.000 0.040 1 24191716 upstream gene variant T/C snv 0.68 1
rs10888501
LCE3E
1.000 0.040 1 152565478 downstream gene variant G/A snv 0.48 1
rs10960680 1.000 0.040 9 12483941 intergenic variant A/C snv 9.4E-02 1
rs10979182
LOC105376214
1.000 0.040 9 108054739 regulatory region variant A/G snv 0.44 1
rs11053802
KLRC1
1.000 0.040 12 10444608 intron variant C/G;T snv 1
rs11059675
LRRC43
1.000 0.040 12 122183779 intron variant G/A snv 0.43 1
rs11121129
LINC01714
1.000 0.040 1 8208035 intron variant G/A snv 0.26 1
rs11135056 1.000 0.040 5 159260273 upstream gene variant C/T snv 0.27 1
rs114934997 1.000 0.040 5 40370622 intergenic variant C/A;T snv 1
rs11575234
STAT2
1.000 0.040 12 56350492 intron variant C/G;T snv 1
rs11652075
CARD14 ; SGSH
0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 1
rs11795343
DDX58
1.000 0.040 9 32523739 intron variant T/C snv 0.41 1
rs118086960
CFL1
1.000 0.040 11 65825973 intron variant A/T snv 0.62 1
rs11922372
LOC107986171
1.000 0.040 3 191162345 intergenic variant T/C snv 0.38 1
rs12118303 1.000 0.040 1 172705957 intergenic variant T/C snv 0.14 1
rs12199223
HLA-B
1.000 0.040 6 31274954 intron variant T/A snv 8.6E-02 1
rs12458130 1.000 0.040 18 8667063 intergenic variant G/A snv 8.9E-02 1
rs12564022
IL23R ; C1orf141
1.000 0.040 1 67205072 intron variant C/T snv 0.30 1
rs12580100 1.000 0.040 12 56045425 upstream gene variant A/G snv 0.14 1
rs12586317
PRORP
1.000 0.040 14 35212966 intron variant T/C snv 0.19 1
rs12650590 1.000 0.040 4 155618869 intergenic variant G/T snv 0.14 1
rs1265181
PSORS1C3
0.925 0.040 6 31188008 intergenic variant G/C snv 0.15 1
rs12895275
RGS6
1.000 0.040 14 72249807 intron variant A/G snv 3.0E-02 1