Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 6
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs10202630 0.882 2 190398199 intergenic variant T/C snv 0.52 4
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4
rs145268310 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 4
rs1549922 0.882 5 159304540 intergenic variant G/A snv 0.56 4
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 4
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs57791671 0.882 3 121889586 upstream gene variant T/A snv 0.38 4
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 4
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 4
rs9356551 0.882 6 166986857 intron variant T/C snv 0.42 4
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 3
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 2
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 2