Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs359457 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 2
rs115575857 1.000 0.200 6 32691868 regulatory region variant A/G snv 1
rs1507153 1.000 0.200 6 78774669 intergenic variant C/A snv 0.32 1
rs1957173 1.000 0.200 14 45937713 intron variant C/T snv 4.6E-02 1
rs7119038 1.000 0.200 11 118867572 intergenic variant G/A snv 0.77 1
rs7999279 1.000 0.200 13 47376590 intergenic variant A/C snv 0.76 1
rs9271573 1.000 0.200 6 32622724 TF binding site variant A/C snv 0.55 1
rs2736345
BLK
0.882 0.280 8 11494976 intron variant A/G snv 0.35 3
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 6
rs4282438
COL11A2P1
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs3135394
HLA-DRA
0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 4
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 5