Source: CURATED ×
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
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 18
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 17
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 11
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11 11
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 11
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 10
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 10
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 9
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs9268853
HLA-DRB9
0.790 0.440 6 32461866 intron variant T/C snv 0.29 9
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs2269426
TNXB
0.807 0.280 6 32108722 intron variant G/A snv 0.35 8
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 8