Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2241883 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs2228314 0.790 0.360 22 41880738 missense variant G/C snv 0.34 0.38 8
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs3774261 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs1800777 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs368234815 0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs17883901 0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs4844880 0.882 0.240 1 209697571 intron variant A/T snv 0.70 4
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs11868035 0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs694539 0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs3816873 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs4823173 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 8
rs2854116 0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs1805096 0.827 0.200 1 65636574 synonymous variant G/A snv 0.46 0.43 6