Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs9368699 0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 7
rs2844509 0.882 0.160 6 31543147 intron variant A/G snv 0.23 6
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs12211410 0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05 5
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs2251396 0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 4
rs6010620 0.701 0.360 20 63678486 intron variant A/C;G snv 4
rs2158177 0.925 0.120 5 132648366 intron variant A/G snv 0.18 4
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3
rs10445308 0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs176095 0.925 0.160 6 32190542 upstream gene variant A/G snv 0.22 3
rs3091307 0.925 0.160 5 132653444 intron variant A/G snv 0.34 3
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 2
rs17728338 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 2
rs13015714 0.882 0.200 2 102355405 intron variant G/T snv 0.77 2
rs6871536 0.827 0.160 5 132634182 intron variant T/C snv 0.24 2
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 2