Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78545931 0.925 0.080 2 102265892 intergenic variant A/G snv 0.16 2
rs7894791 1.000 0.080 10 8549406 intergenic variant C/A snv 0.36 2
rs7927044 0.925 0.080 11 127891771 intergenic variant G/A snv 2.3E-02 2
rs850637 0.925 0.080 X 13005622 intergenic variant G/A snv 0.43 2
rs9815663 0.925 0.080 3 3573203 intron variant C/T snv 0.22 2
rs9893132 0.925 0.080 17 40598769 upstream gene variant A/G snv 0.59 2
rs9895436 0.925 0.080 17 45380520 intergenic variant G/A snv 0.49 2
rs10519031 1.000 0.080 15 59890806 regulatory region variant T/C snv 2.2E-02 1
rs11021111 1.000 0.080 11 95270099 intergenic variant C/G snv 4.3E-02 1
rs16929097 1.000 0.080 9 12521826 intergenic variant G/A snv 4.7E-02 1
rs17033506 1.000 0.080 3 35598334 intergenic variant G/T snv 2.8E-02 1
rs17111521 1.000 0.080 14 41164182 intergenic variant C/A snv 6.7E-02 1
rs17218161 1.000 0.080 4 58347679 intergenic variant T/C snv 4.3E-03 1
rs1931704 1.000 0.080 10 127541545 intergenic variant G/A snv 0.28 1
rs2311978 1.000 0.080 X 76568453 intergenic variant C/T snv 0.58 1
rs2378383 1.000 0.080 9 79424447 intergenic variant A/C;G;T snv 1
rs34880821 1.000 0.080 7 22735831 downstream gene variant G/A snv 0.21 1
rs3893044 1.000 0.080 17 39946763 downstream gene variant T/C snv 0.63 1
rs486512 1.000 0.080 17 39209446 downstream gene variant C/T snv 5.5E-02 1
rs6054973 1.000 0.080 20 7405311 intergenic variant T/C snv 4.8E-02 1
rs6954667 1.000 0.080 7 22740703 intergenic variant C/A snv 0.27 1
rs7045156 1.000 0.080 9 79311350 intergenic variant T/C snv 3.6E-02 1
rs7209742 1.000 0.080 17 39952455 upstream gene variant A/G snv 0.69 1
rs7974135 1.000 0.080 12 107977536 intergenic variant G/A snv 1.1E-02 1
rs8029377 1.000 0.080 15 59899786 intergenic variant A/C snv 3.1E-02 1