Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 5
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 4
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 3