Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10078434 1.000 0.080 5 138496342 intergenic variant A/T snv 0.13 1
rs1022442 1.000 0.080 21 20983528 intergenic variant G/A snv 0.40 1
rs10405693 1.000 0.080 19 44823407 downstream gene variant C/T snv 0.28 1
rs10407439 1.000 0.080 19 44838691 intergenic variant A/G snv 0.69 1
rs10412413 1.000 0.080 19 44824052 downstream gene variant C/T snv 0.30 1
rs10455152 1.000 0.080 6 85308630 intergenic variant A/C snv 0.29 1
rs1081106 1.000 0.080 19 44910109 non coding transcript exon variant T/C snv 7.2E-02 1
rs10850408 1.000 0.080 12 114942588 intergenic variant C/T snv 0.31 1
rs11062987 1.000 0.080 12 4063960 intergenic variant A/G snv 4.6E-02 1
rs111371860 1.000 0.080 19 44842530 upstream gene variant A/T snv 5.1E-02 1
rs11168036 1.000 0.080 5 140327854 downstream gene variant T/G snv 0.48 1
rs112262807 1.000 0.080 19 44828429 intergenic variant C/T snv 0.26 1
rs113118940 1.000 0.080 20 23514209 intron variant C/T snv 1.1E-02 1
rs113524839 1.000 0.080 5 84788958 intergenic variant C/T snv 5.9E-02 1
rs115641191 1.000 0.080 4 102133052 intergenic variant C/T snv 6.2E-03 1
rs115786578 1.000 0.080 20 34149795 intergenic variant G/A;C;T snv 1
rs115809613 1.000 0.080 4 98971324 intron variant A/G snv 4.8E-03 1
rs11603136 1.000 0.080 11 86163280 regulatory region variant A/C snv 0.41 1
rs116938548 1.000 0.080 12 4699085 intron variant C/T snv 4.2E-04 1
rs117483990 1.000 0.080 12 89830937 intron variant T/G snv 5.9E-03 1
rs11749176 1.000 0.080 5 44145829 intergenic variant T/A;G snv 1
rs117908734 1.000 0.080 14 98492717 upstream gene variant C/T snv 8.1E-03 1
rs118071777 1.000 0.080 7 88614935 intron variant G/A snv 4.2E-03 1
rs118152978 1.000 0.080 8 126341293 intergenic variant A/G;T snv 1
rs11827324 1.000 0.080 11 60332439 upstream gene variant A/G snv 0.30 1