Disease: Acquired Immunodeficiency Syndrome
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
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs1233579 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 3
rs3131093 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 3
rs3749971
OR12D3 ; OR5V1
0.925 0.160 6 29374998 missense variant G/A snv 5.5E-02 5.7E-02 3
rs13194504 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 2