Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs191252491
ALDH2
0.882 12 111773070 intron variant A/T snv 7.1E-03 4
rs72920202
JAK1
0.882 1 64895266 intron variant A/T snv 0.15 4
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs142647938
KCNH7
0.882 2 162516642 intron variant C/A;T snv 4
rs7005834
CCN4
0.827 0.160 8 133201961 intron variant C/A;T snv 4
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs13380830
RAB5C
0.882 17 42145640 intron variant C/G snv 0.29 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs36001488
ATG16L1
0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs62131887 0.724 0.240 19 10476920 intergenic variant C/T snv 0.37 14
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14