Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs2156875
HLA-B
0.882 0.200 6 31349570 intron variant C/T snv 0.50 6
rs6906846
HLA-B ; USP8P1
0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
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
rs2596501
HLA-B
0.882 0.200 6 31353434 intron variant C/T snv 0.57 3
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 3
rs3132486
HLA-B
0.925 0.160 6 31275393 intron variant G/A snv 0.49 2
rs1634747
HLA-B
1.000 0.120 6 31314099 intron variant G/A snv 0.41 1
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53 1
rs9265797
HLA-B
1.000 0.120 6 31340853 intron variant G/A snv 0.30 1
rs3094682
HLA-B ; LOC112267902 ; LINC02571
1.000 0.120 6 31296684 intron variant A/C;T snv 1
rs3094691
LOC112267902 ; HLA-B
1.000 0.120 6 31306916 intron variant G/A snv 0.51 1
rs7755852
LOC112267902 ; HLA-B
1.000 0.120 6 31310211 intron variant A/G snv 0.49 1