Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs4672497 2 62296430 TF binding site variant C/G;T snv 5
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs78744187 19 33263642 intergenic variant C/T snv 6.8E-02 5
rs7955734 12 4223993 intergenic variant C/G snv 0.22 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 4
rs532591337 19 12459271 intron variant G/A snv 4.9E-05 4
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs74929147 19 18302251 downstream gene variant G/A;C snv 4
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs10849023 12 4223312 intergenic variant C/T snv 0.22 3
rs35259020 9 134085798 intergenic variant CT/- delins 0.18 3
rs4916483 3 196180782 intergenic variant T/C snv 0.12 3
rs5872391 5 154655826 intergenic variant AA/-;A delins 0.35 3
rs632057 6 139512875 intron variant T/G snv 0.57 3