Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1181860747 0.776 0.240 19 7122961 missense variant C/T snv 10
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1223493898 0.851 0.120 20 44406090 missense variant G/A;C snv 5
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
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
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
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16