Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3790567
IL12RB2
0.851 0.240 1 67356694 intron variant A/G snv 0.61 1
rs485499
LINC01100 ; IL12A-AS1
0.925 0.080 3 160028076 intron variant T/C snv 0.29 1
rs6890853
LOC105374724
0.925 0.080 5 35852209 upstream gene variant G/A snv 0.25 1
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 1
rs10931468
NAB1
0.925 0.080 2 190673836 intron variant C/A;G;T snv 1
rs1372072
PLCL2
0.851 0.200 3 16913767 intron variant G/A snv 0.35 1
rs911263
RAD51B
0.851 0.200 14 68286876 intron variant C/T snv 0.57 1
rs538147
RPS6KA4
0.925 0.080 11 64362250 intron variant G/A snv 0.29 1
rs3745516
SPIB
0.925 0.080 19 50423485 intron variant A/G snv 0.62 1