Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11160753 14 103541163 downstream gene variant C/G;T snv 1
rs11204538 1 247882970 downstream gene variant C/T snv 0.55 1
rs112390170 6 31267969 downstream gene variant G/A snv 1
rs11855741 15 31261168 intergenic variant G/C snv 6.4E-02 1
rs11929092 3 196176059 intergenic variant T/C snv 0.39 1
rs12135894 1 3811497 downstream gene variant C/A;T snv 1
rs12412214 10 99516499 intergenic variant G/A snv 0.26 1
rs12582170 12 53364047 intergenic variant A/G snv 0.69 1
rs13011075 2 68412181 intergenic variant A/C snv 0.26 1
rs1317931 11 128044858 regulatory region variant A/G snv 0.76 1
rs139164185 1 198583770 intergenic variant G/A;C snv 1
rs140484951 6 29178695 upstream gene variant T/C snv 1
rs150340932 X 55552777 intergenic variant T/C snv 1
rs172629 4 54541595 intergenic variant C/G snv 0.17 1
rs184739375 13 72701469 upstream gene variant T/C snv 1.9E-03 1
rs198833 6 26114280 downstream gene variant G/A snv 0.87 1
rs218256 4 54536242 intergenic variant C/G snv 0.38 1
rs2340727 1 161976937 intergenic variant A/G snv 0.33 1
rs2703485 4 54571325 TF binding site variant T/C snv 0.45 1
rs2904967 11 65324138 intron variant G/A;C snv 0.14 1
rs34165383 5 154646913 intergenic variant C/G snv 8.9E-02 1
rs36092669 1 114519906 intergenic variant T/C snv 0.33 1
rs55794721 1 25235176 upstream gene variant G/A snv 0.28 1
rs5995385 22 37123824 downstream gene variant T/C snv 0.46 1
rs6092477 20 57416639 regulatory region variant G/A snv 0.36 1