Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3745516
SPIB
0.925 0.080 19 50423485 intron variant A/G snv 0.62 1
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
rs4938534
BTG4 ; POU2AF1
0.925 0.080 11 111404408 intron variant G/A snv 0.56 1
rs538147
RPS6KA4
0.925 0.080 11 64362250 intron variant G/A snv 0.29 1
rs6441286
IL12A-AS1
0.925 0.080 3 160011091 intron variant T/G snv 0.36 1
rs8017161
EXOC3L4
0.925 0.080 14 103096858 intron variant G/A snv 0.38 1
rs911263
RAD51B
0.851 0.200 14 68286876 intron variant C/T snv 0.57 1
rs968451 0.925 0.080 22 39274846 intron variant G/T snv 0.18 1