Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 4
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 4
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 2
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 2
rs10800309 0.925 0.120 1 161502368 upstream gene variant A/G;T snv 2
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G 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
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
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