Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 11
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12 10
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 7
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs11614178
IFNG-AS1 ; LOC107984526
0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs12718244
SPATA48
0.827 0.120 7 50136058 intron variant G/A snv 0.33 0.33 6
rs12942547
STAT3
0.807 0.200 17 42375526 intron variant A/G;T snv 6
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 6
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6