Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs37369 0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 9
rs4740 0.827 0.240 19 4236999 missense variant G/A snv 0.34 0.39 8
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 7