Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs7530511
IL23R ; C1orf141
0.742 0.400 1 67219704 missense variant T/A;C snv 0.88 12
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
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
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 5
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs10553577
STAT4
1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins 1
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs359457 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 2
rs6579837
TNIP1
1.000 0.200 5 151055333 intron variant G/T snv 0.11 1
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs4282438
COL11A2P1
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6