Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs13114738 0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1320702652 0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2549513
MAF
0.851 0.080 16 79516830 downstream gene variant C/A;T snv 4
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs4704221 0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4905014 0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs7081476 0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs7115242 0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
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
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16