Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 8
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 7
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 7
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
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 7
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 7
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 7
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 6
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs4703855 0.827 0.120 5 72398072 regulatory region variant C/T snv 0.24 6
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6