Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 5
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1884444
IL23R ; C1orf141
0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs200820567 0.882 0.160 6 137908903 intergenic variant T/A snv 2.0E-02 4
rs2132039
UGT2B28
0.925 0.120 4 69293669 intron variant T/A;C snv 2
rs2230926
TNFAIP3
0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs2296651
SLC10A1
0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs2617160
KLRC4-KLRK1 ; LOC101928100
1.000 0.080 12 10392998 intron variant A/C;T snv 1
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs2853953 1.000 0.080 6 31267728 downstream gene variant G/A snv 0.20 1
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs3106796
COL3A1 ; LOC105373791
0.882 0.160 2 188985047 non coding transcript exon variant A/G snv 0.35 3
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 8
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs3759333
LTBR
0.882 0.120 12 6382781 intron variant C/G;T snv 3
rs3775290
TLR3
0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 15