Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6906662
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32298729 intron variant G/A snv 6.8E-02 6
rs2219893 0.925 0.120 6 32801886 intergenic variant T/C snv 0.33 5
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2621373 0.925 0.120 6 32797353 TF binding site variant T/A;C;G snv 5
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs719654 0.925 0.120 6 32784362 intergenic variant G/A snv 0.21 5
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs9378200 0.925 0.120 6 31605150 intergenic variant T/C snv 5.4E-02 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2248372
HCP5
0.925 0.120 6 31478689 non coding transcript exon variant G/A snv 0.32 5
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 5
rs1058026
HLA-B
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 5
rs4386816
HLA-B
0.925 0.120 6 31279358 intron variant T/C snv 0.17 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
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