Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 7
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs13132308
IL21-AS1
0.807 0.160 4 122629959 intron variant A/G snv 0.10 6
rs13407913
ADCY3
0.827 0.120 2 24874775 intron variant A/G snv 0.54 6
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs2816958
NR5A2
0.827 0.120 1 200132792 intron variant A/G snv 0.84 6
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36 6
rs7552167 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 6
rs7608910
PUS10
0.827 0.120 2 60977721 intron variant A/G snv 0.37 6
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs11691685
TEX41
0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02 5
rs12075255
IL19
0.827 0.120 1 206788283 intron variant A/G snv 0.74 5
rs12694846
SP140
0.827 0.120 2 230283413 intron variant A/G snv 0.20 5
rs17229679
LOC105373831
0.827 0.120 2 198696033 intron variant A/G snv 3.0E-02 5
rs2026029
FNDC3A
0.827 0.120 13 49021195 intron variant A/G snv 0.58 5
rs2042011 0.827 0.120 8 128215706 upstream gene variant A/G snv 0.39 5
rs2357623 0.827 0.120 16 50660100 upstream gene variant A/G snv 0.71 5
rs2666218
ASAP2
0.827 0.120 2 9262859 intron variant A/G snv 0.32 5
rs3118471
IL2RA
0.827 0.120 10 6060794 intron variant A/G snv 0.24 5
rs72871627
IFIH1
0.827 0.120 2 162280432 intron variant A/G snv 7.1E-03 5
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 5
rs7915475
ZNF365
0.827 0.120 10 62621908 intron variant A/G snv 0.28 5
rs79568124 0.827 0.120 1 161533059 intron variant A/G snv 8.8E-02 5