Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs3759333
LTBR
0.882 0.120 12 6382781 intron variant C/G;T snv 3
rs2132039
UGT2B28
0.925 0.120 4 69293669 intron variant T/A;C snv 2
rs9366816
HLA-DPA3 ; LOC105375021
0.925 0.080 6 33136398 intron variant T/C snv 0.22 2
rs2617160
KLRC4-KLRK1 ; LOC101928100
1.000 0.080 12 10392998 intron variant A/C;T snv 1
rs4845384
ADAR
1.000 0.080 1 154615193 intron variant A/G snv 0.69 1
rs4935047
MBL2
1.000 0.080 10 52770307 intron variant A/G snv 0.49 1
rs7712322
POLR3G
1.000 0.080 5 90482078 intron variant C/A;T snv 1
rs78900671
COL22A1
1.000 0.080 8 138653967 intron variant G/A;C snv 1
rs9287655
NBAS
1.000 0.080 2 15245360 intron variant C/T snv 0.45 1
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs200820567 0.882 0.160 6 137908903 intergenic variant T/A snv 2.0E-02 4
rs148314165 0.925 0.160 6 137908902 intergenic variant T/- delins 2.0E-02 3
rs61886277
PLCE1
1.000 0.080 10 94012060 intergenic variant C/T snv 0.19 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262