Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 7
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs3136534 0.807 0.240 4 122448621 downstream gene variant T/G snv 0.29 6
rs4880213 0.827 0.160 9 137136549 upstream gene variant C/G;T snv 6
rs9461799 0.807 0.360 6 32721752 downstream gene variant T/C snv 0.37 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 5
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 5
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 5
rs6457620 0.882 0.200 6 32696222 intergenic variant G/C snv 0.52 5
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 5
rs9469220 0.827 0.160 6 32690533 TF binding site variant G/A snv 0.53 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 4
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 4