Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114846446
LINC01250
0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078
C1orf141 ; IL23R
0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs2066363
ADGRL2
0.724 0.240 1 81771892 intron variant C/T snv 0.71 14
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 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
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs6689858
CRB1
0.724 0.240 1 197406337 intron variant T/C snv 0.39 14
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs7100025
ANKRD30A ; LINC00993
0.724 0.240 10 37303610 intron variant G/A snv 0.68 14
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 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
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 12