Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10887800 0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1186757238 1.000 0.040 5 59039089 5 prime UTR variant A/C snv 2
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs147603016 0.925 0.160 5 177093286 synonymous variant G/A;C snv 1.5E-04; 8.2E-06 3
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57