Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs757537938
C2 ; C2-AS1 ; CYP21A2
0.882 0.200 6 31943672 missense variant A/C snv 4.1E-06 3
rs1805011
IL4R
0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs5744174
TLR5
0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs9277535
HLA-DPB1
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs120074192
KCNQ1
0.763 0.120 11 2527959 missense variant A/G snv 10
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs2284553
IFNGR2
0.776 0.240 21 33404389 intron variant A/G snv 0.69 9
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 8
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs8177832
APOBEC3G
0.851 0.160 22 39081561 missense variant A/G snv 5.9E-02 0.14 5
rs9277378
HLA-DPB1 ; HLA-DPA1
0.827 0.320 6 33082502 intron variant A/G snv 0.40 5
rs2072906
PNPLA3
0.851 0.160 22 43937292 intron variant A/G snv 0.25 0.20 4
rs2532932 0.925 0.160 6 30927667 downstream gene variant A/G snv 0.74 2
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10