Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 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
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
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
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 11
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 11
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 10
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 10