Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11583043
DPH5
1.000 0.040 1 101000498 intron variant C/T snv 0.28 1
rs13107612
BANK1
0.827 0.120 4 101818823 intron variant C/T snv 0.31 5
rs4851529
LOC107985926
0.827 0.120 2 102030838 downstream gene variant G/A snv 0.44 5
rs10185424 0.925 0.040 2 102046427 intron variant T/G snv 0.62 2
rs2310173 0.925 0.080 2 102047167 intron variant T/C;G snv 2
rs871656
IL1R1
0.827 0.120 2 102154822 intron variant T/A;C snv 5
rs12987977
IL18R1
0.827 0.120 2 102358876 intron variant T/G snv 0.31 5
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 2
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs3740415
ACTR1A ; MFSD13A
1.000 0.040 10 102472959 3 prime UTR variant G/A snv 0.48 0.48 1
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 5
rs3774959
NFKB1
0.925 0.080 4 102589957 intron variant G/A snv 0.34 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 5
rs35018800
TYK2
0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 5
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 1
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs35074907
KEAP1
0.807 0.160 19 10489742 synonymous variant G/A snv 1.9E-02 1.5E-02 6
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs11750385
LINC02213
0.827 0.120 5 10521556 intron variant G/A;T snv 5
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs4946717
PRDM1
0.827 0.120 6 106026874 intron variant C/A;G;T snv 6