Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 12
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 12
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 9
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs1182188
GNA12
0.827 0.120 7 2830351 intron variant T/C snv 0.26 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 8
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 8
rs11229555
GLYAT
0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 7
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs2266961
UBE2L3
0.807 0.160 22 21574308 intron variant C/G snv 0.18 7
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45 7
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs11614178
IFNG-AS1 ; LOC107984526
0.827 0.120 12 68114342 intron variant G/A;T snv 0.26 6
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 6
rs1267499
LOC101928354
0.807 0.160 6 14715651 intron variant T/A;C snv 6
rs12718244
SPATA48
0.827 0.120 7 50136058 intron variant G/A snv 0.33 0.33 6