Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6
rs241447
TAP2
0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 5
rs3869068
ZNRD1ASP
0.925 6 30036275 intron variant C/T snv 0.17 4
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53 1
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 1