Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
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
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs1004819
C1orf141 ; IL23R
0.776 0.360 1 67204530 intron variant G/A snv 0.30 9
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs1085308048
PTEN
0.851 0.320 10 87933175 stop gained T/G snv 6
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 6
rs3757387
IRF5
0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 6
rs4282438
COL11A2P1
0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48 5
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
rs3135394
HLA-DRA
0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 4
rs2736345
BLK
0.882 0.280 8 11494976 intron variant A/G snv 0.35 3
rs359457 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 2
rs3823536
IRF5
0.925 0.280 7 128939612 intron variant G/A snv 0.40 2