Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs7765379 0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10 3
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 3
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 2
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 2
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 2
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 2
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 2
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs224136 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 2
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 2
rs3091316 1.000 0.040 17 34266955 upstream gene variant G/A;C snv 2
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 2
rs4409764 0.925 0.040 10 99524480 upstream gene variant T/A;G snv 2
rs4574921 0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80 2
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 2
rs6478106 0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34 2