Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs52820871 0.827 0.160 18 60371599 missense variant T/G snv 6.9E-03 7.6E-03 6
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs6136 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs6564851 0.882 0.120 16 81230992 intergenic variant T/G snv 0.48 5
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs9402571 0.882 0.080 6 134167822 downstream gene variant T/G snv 0.22 4
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1037733674 0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1308346790 0.925 0.080 4 26430444 missense variant T/C snv 4.0E-06 3
rs137852785 0.925 0.080 13 27920190 missense variant T/C snv 1.1E-04 1.0E-04 3
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1570056 0.925 0.080 6 136738789 intron variant T/C snv 0.52 3
rs17107315 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs17366743 0.807 0.280 3 186854300 missense variant T/C snv 2.2E-02 2.1E-02 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34