Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs2284178
HCP5
0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 6
rs1058026
HLA-B
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 5
rs1894406
HLA-DOB
0.925 0.120 6 32819279 intron variant C/G;T snv 5
rs2071472
HLA-DOB
0.925 0.120 6 32816843 intron variant C/T snv 0.34 0.27 5
rs2071474
HLA-DOB
0.925 0.120 6 32814805 intron variant C/T snv 0.27 5
rs2219893 0.925 0.120 6 32801886 intergenic variant T/C snv 0.33 5
rs2248372
HCP5
0.925 0.120 6 31478689 non coding transcript exon variant G/A snv 0.32 5
rs2249742
HLA-B ; HLA-C
0.925 0.120 6 31272944 intron variant C/T snv 0.50 5
rs2395471
HLA-B ; HLA-C
0.925 0.120 6 31272915 intron variant G/A snv 0.47 5
rs241440
TAP2
0.925 0.120 6 32829584 intron variant C/G;T snv 0.30 5
rs241452
TAP2
0.925 0.120 6 32828569 3 prime UTR variant T/C snv 0.26 5
rs2534678
MICB ; MICB-DT
0.925 0.120 6 31496186 intron variant G/A;T snv 5
rs2621373 0.925 0.120 6 32797353 TF binding site variant T/A;C;G snv 5
rs2857106
HLA-DOB
0.925 0.120 6 32819793 intron variant T/C snv 0.19 5
rs2905722
MICB-DT
0.925 0.120 6 31481550 intron variant A/G snv 0.88 5
rs4386816
HLA-B
0.925 0.120 6 31279358 intron variant T/C snv 0.17 5
rs719654 0.925 0.120 6 32784362 intergenic variant G/A snv 0.21 5
rs9378200 0.925 0.120 6 31605150 intergenic variant T/C snv 5.4E-02 5
rs13330041
CLEC16A
1.000 0.120 16 10994951 intron variant G/A snv 0.25 2
rs1419675 1.000 0.120 6 30124930 intergenic variant G/T snv 0.74 2
rs16898264 1.000 0.120 6 32709375 upstream gene variant G/A snv 0.34 2
rs17211510
HLA-DQA1
1.000 0.120 6 32634653 intron variant C/A snv 0.26 2
rs17533090 1.000 0.120 6 32622945 TF binding site variant G/T snv 0.16 2
rs17673553
CLEC16A
1.000 0.120 16 11148049 intron variant A/G snv 0.18 2