Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11306716 0.827 0.120 2 203843041 intergenic variant T/-;TT delins 5
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs114202211
HIPK1
0.827 0.120 1 113943285 intron variant T/C snv 8.1E-03 5
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 1
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs114934997 1.000 0.040 5 40370622 intergenic variant C/A;T snv 1
rs11574938
ITGAL
0.827 0.120 16 30474072 missense variant G/A;C snv 0.62 6
rs11575234
STAT2
1.000 0.040 12 56350492 intron variant C/G;T snv 1
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11593576
ZMIZ1
0.925 0.040 10 79256139 intron variant C/T snv 0.29 2
rs116046827
BSN
0.827 0.120 3 49618715 intron variant T/C snv 8.6E-03 5
rs11614178
IFNG-AS1 ; LOC107984526
0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs11616188 0.827 0.120 12 6393576 upstream gene variant G/A snv 0.30 5
rs11624293
LINC01147
0.827 0.120 14 88022477 intron variant T/C snv 0.13 5
rs11649613
LOC107984859
0.827 0.120 16 11225500 downstream gene variant C/T snv 0.37 5
rs11652075
CARD14 ; SGSH
0.882 0.040 17 80205094 missense variant C/T snv 0.41 0.40 1
rs11675538 0.827 0.120 2 65459327 intron variant C/T snv 0.29 5
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 5
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02 5
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11749040 0.827 0.120 5 40396323 regulatory region variant G/A snv 0.15 5
rs11749391
IRGM
0.827 0.120 5 150849504 intron variant T/C snv 0.21 5
rs11750385
LINC02213
0.827 0.120 5 10521556 intron variant G/A;T snv 5