Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34557412
TNFRSF13B
0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 4
rs2066844
NOD2
0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 5
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 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
rs34884278 0.724 0.240 1 172869708 intron variant C/T snv 0.63 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 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
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs7100025
ANKRD30A ; LINC00993
0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs36001488
ATG16L1
0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14