Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs9901869 0.925 0.120 17 47497840 intergenic variant G/A snv 0.56 1
rs9889296 0.827 0.120 17 34243528 intergenic variant G/A snv 0.33 6
rs9797244
NOS2
0.827 0.120 17 27770105 intron variant T/C snv 0.19 5
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 5
rs9554587 0.827 0.120 13 99388400 downstream gene variant A/G snv 0.17 5
rs9494840 0.827 0.120 6 137641937 regulatory region variant T/A snv 4.3E-05 5
rs9491891 0.827 0.120 6 127956006 intergenic variant A/G snv 0.12 5
rs9438876
RUNX3
1.000 0.040 1 24914625 intron variant A/G snv 0.53 1
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 6
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 6
rs928722 0.827 0.120 6 137652695 intergenic variant C/T snv 0.16 5
rs925255
FOSL2 ; FLJ31356
0.827 0.120 2 28391927 intron variant C/T snv 0.38 6
rs924080 0.882 0.240 1 67294457 intergenic variant T/C snv 0.45 1
rs871656
IL1R1
0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs860262
JAZF1
0.807 0.200 7 28154778 intron variant C/A;T snv 0.41 6
rs8176786
NELL1
0.925 0.040 11 20937848 missense variant C/T snv 4.5E-02 3.7E-02 1
rs8070463 0.925 0.120 17 47691470 upstream gene variant T/C snv 0.54 2
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11 5
rs80174646
IL23R
0.827 0.120 1 67242472 intron variant G/T snv 5.8E-02 5
rs8006884
LOC101927178 ; PPP2R3C ; FAM177A1
0.827 0.120 14 35094005 intron variant T/C snv 0.36 5
rs79568124 0.827 0.120 1 161533059 intron variant A/G snv 8.8E-02 5
rs7954567
LTBR
0.925 0.080 12 6381959 intron variant G/A snv 0.25 2
rs79493594
PKIG
0.827 0.120 20 44561731 intron variant C/T snv 2.1E-02 5