Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1020608562 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10489177 0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs1057518903 0.882 0.160 11 64807890 splice region variant C/- delins 6
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs121909244 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1337503417 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs17118 0.925 0.120 3 38362981 missense variant C/A;T snv 0.29 4
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2071410 0.882 0.160 15 90877710 intron variant C/A;G;T snv 7
rs2106261 0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99