Disease: Acquired Immunodeficiency Syndrome
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs3815087
PSORS1C1
0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 7
rs2844513 0.925 0.120 6 31420437 intron variant G/A snv 0.53 6
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs3823418
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 0.23 6
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6