Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs9300039 0.851 0.160 11 41893816 intergenic variant C/A snv 9.8E-02 4
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs3890182 0.925 0.120 9 104885374 intron variant G/A;T snv 5
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs9282541 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs12495941 0.851 0.280 3 186850391 intron variant G/T snv 0.35 5
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs7649121 0.882 0.160 3 186850996 intron variant A/T snv 0.17 3
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17366568 0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 6
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs3774261 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65