Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs12603332 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 7
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 5
rs1799962
IL9
0.925 0.080 5 135896167 upstream gene variant T/C;G snv 7.2E-02 3
rs1872387 0.925 0.120 2 138964859 intron variant G/C snv 0.55 2
rs1921622 1.000 0.080 2 102349607 intron variant G/A snv 0.42 2
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs11688
JUN
1.000 0.080 1 58782321 synonymous variant C/T snv 5.3E-02 9.7E-02 1
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2069885
IL9
0.851 0.120 5 135892476 missense variant G/A;C snv 0.11 5
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48