Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17489282 1.000 0.040 8 19995007 regulatory region variant C/T snv 0.25 5
rs180349 0.925 0.200 11 116741111 intergenic variant A/C;T snv 5
rs1919484 1.000 0.040 8 20012165 intergenic variant G/A snv 0.23 5
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 5
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 4
rs2741027 1.000 0.040 2 233609365 downstream gene variant G/A snv 0.22 4
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 4
rs7013777 1.000 0.040 8 20020845 intergenic variant T/C;G snv 4
rs7461115 1.000 0.040 8 20014029 intergenic variant C/A;G snv 0.37 4
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 4
rs11600380 1.000 0.040 11 116799466 intergenic variant T/C snv 6.6E-02 3
rs1423096 0.925 0.080 19 7674291 upstream gene variant T/C snv 0.92 3
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 3
rs7841189 1.000 0.040 8 19987865 TF binding site variant C/T snv 0.15 3
rs11774572 1.000 0.040 8 11589291 regulatory region variant C/G;T snv 2
rs13189262 1.000 0.040 5 57978493 intergenic variant G/T snv 0.16 2
rs16885704 1.000 0.040 6 74829426 regulatory region variant A/G snv 6.1E-02 2
rs2963791 1.000 0.040 5 3844427 regulatory region variant C/A snv 0.80 2
rs359935 1.000 0.040 1 89517625 intron variant G/A;T snv 2
rs4922117 1.000 0.040 8 19995075 regulatory region variant T/A;C;G snv 0.25 2
rs5945326 0.925 0.080 X 153634467 regulatory region variant A/G snv 0.25 2
rs6585514 1.000 0.040 10 118836874 intron variant A/G snv 0.62 2
rs6711016 1.000 0.040 2 20923592 intergenic variant C/A snv 0.19 2
rs6947830 0.925 0.080 7 15025359 intergenic variant G/A;C snv 2
rs7865146 1.000 0.040 9 127857358 upstream gene variant C/G;T snv 2