Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 1
rs1800693
TNFRSF1A
0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 2
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
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs11117432 0.851 0.200 16 85985665 upstream gene variant G/A snv 0.15 1
rs6890853
LOC105374724
0.925 0.080 5 35852209 upstream gene variant G/A snv 0.25 1
rs860413 0.925 0.080 5 35942940 upstream gene variant A/C snv 0.23 1
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 1