Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 1
rs7665590
EIF4E
0.925 0.080 4 98875633 3 prime UTR variant T/C snv 0.56 1
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs8017161
EXOC3L4
0.925 0.080 14 103096858 intron variant G/A snv 0.38 1
rs860413 0.925 0.080 5 35942940 upstream gene variant A/C snv 0.23 1
rs911263
RAD51B
0.851 0.200 14 68286876 intron variant C/T snv 0.57 1
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 4
rs968451 0.925 0.080 22 39274846 intron variant G/T snv 0.18 1