Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs149014830 1.000 0.080 5 121540642 intergenic variant C/A;G snv 1.3E-02 1
rs186920977 1.000 0.080 2 56422795 intergenic variant G/A snv 1.1E-02 1
rs61858823 1.000 0.080 10 65095495 intergenic variant G/A snv 1.3E-02 1
rs6582630 1.000 0.080 12 38349706 intergenic variant G/A snv 0.62 1
rs6694270 1.000 0.080 1 18793883 intergenic variant A/G snv 0.26 1
rs72696020 1.000 0.080 14 88105563 intergenic variant G/A snv 9.9E-03 1
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
rs9274407
HLA-DQB1
0.925 0.120 6 32665055 missense variant A/C;T snv 0.77 3
rs597480
SYTL2
1.000 0.080 11 85725825 missense variant G/C;T snv 0.59; 3.2E-05 1
rs2395029
HCP5
0.790 0.320 6 31464003 non coding transcript exon variant T/G snv 2.7E-02 2.4E-02 12
rs112655218
RAB31
1.000 0.080 18 9841518 non coding transcript exon variant G/A snv 5.0E-02 1
rs17036170
PPARG
1.000 0.080 3 12288912 5 prime UTR variant G/A snv 1.1E-02 2
rs114577328
HLA-A
1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 2