Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7538876 0.807 0.120 1 17395867 intron variant G/A snv 0.37 6
rs801114 0.827 0.120 1 228862088 downstream gene variant T/G snv 0.48 5
rs891835 0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs866460345 0.882 0.120 7 55143362 missense variant C/T snv 4
rs2269432 0.882 0.120 3 50296800 missense variant T/A;G snv 0.13 3
rs258322 0.925 0.120 16 89689495 intron variant A/G;T snv 3
rs4785763 0.925 0.120 16 90000528 non coding transcript exon variant A/C;T snv 3
rs1572072 1.000 0.120 13 23553071 intergenic variant G/T snv 0.36 2
rs189897 1.000 0.120 3 37477054 intron variant T/A snv 0.13 2
rs200046052 1.000 0.120 3 49902693 missense variant C/G;T snv 1.8E-04; 3.6E-05 2
rs2305806 1.000 0.120 19 6754996 synonymous variant T/C snv 0.30 0.35 2
rs2517713 1.000 0.120 6 29950322 downstream gene variant G/A;T snv 2
rs28421666 1.000 0.120 6 32624960 upstream gene variant A/G snv 6.9E-02 2
rs2860580 1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv 2
rs3129055 1.000 0.120 6 29702484 regulatory region variant A/G snv 0.24 2
rs417162 1.000 0.120 6 29948728 downstream gene variant C/T snv 0.66 2
rs770251749 1.000 0.120 6 54121506 missense variant A/C snv 4.0E-06 2
rs9510787 1.000 0.120 13 23631056 intron variant A/G snv 0.20 2
rs10163267 1.000 0.120 16 83940313 intron variant G/A;C snv 1
rs10496040 1.000 0.120 2 55080510 5 prime UTR variant C/A snv 9.1E-02 1
rs1059449 1.000 0.120 6 29942921 missense variant G/A snv 6.1E-02 9.0E-02 1
rs11158728 1.000 0.120 14 68295488 intron variant G/A;C;T snv 1
rs11237828 1.000 0.120 11 79422176 mature miRNA variant T/C snv 0.12 0.22 1
rs115214213 1.000 0.120 11 35231896 3 prime UTR variant T/C snv 4.9E-03 1
rs117465650 1.000 0.120 2 55050090 missense variant C/T snv 0.12 6.1E-02 1