Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 5
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv 5
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs142647938
KCNH7
0.882 2 162516642 intron variant C/A;T snv 4
rs1800601
NTRK1 ; SH2D2A
0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4