Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs485497
IL12A-AS1
0.925 0.200 3 160001345 intron variant A/C;G snv 2
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
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
rs115575857 1.000 0.200 6 32691868 regulatory region variant A/G snv 1
rs2201841
C1orf141 ; IL23R
0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs10553577
STAT4
1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1507153 1.000 0.200 6 78774669 intergenic variant C/A snv 0.32 1
rs17074492
LOC105370283
1.000 0.200 13 81587764 intergenic variant C/A;T snv 1
rs5029939
TNFAIP3
0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs774359492
WDHD1
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 7
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 6
rs359457 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 2
rs17339836
TNPO3
1.000 0.200 7 129041008 intron variant C/T snv 9.0E-02 1
rs1957173 1.000 0.200 14 45937713 intron variant C/T snv 4.6E-02 1
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52