Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs7632505 0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16