Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4649203 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 1
rs4845454 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 1
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 1
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 1
rs6677595 1.000 0.040 1 152617711 downstream gene variant C/G;T snv 1
rs7536201
RUNX3
0.925 0.040 1 24966593 upstream gene variant T/C;G snv 1
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs702873
LINC01185
0.882 0.120 2 60854407 intron variant C/T snv 0.35 3
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 2
rs17716942
KCNH7
0.925 0.040 2 162404181 intron variant T/C snv 9.6E-02 1
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19 1
rs4676406 0.827 0.120 2 240639691 intergenic variant G/T snv 0.53 1
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 1
rs62149416
LINC01185
0.925 0.040 2 60856371 intron variant T/C snv 0.26 1
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 1
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 1
rs925255
FOSL2 ; FLJ31356
0.827 0.120 2 28391927 intron variant C/T snv 0.38 1
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs16861329
ST6GAL1
0.882 0.160 3 186948673 intron variant C/T snv 0.13 1