Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3900940 0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs7692387 0.925 0.080 4 155714157 intron variant G/A snv 0.16 5
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1186757238 1.000 0.040 5 59039089 5 prime UTR variant A/C snv 2
rs145302848 1.000 0.040 5 177093265 synonymous variant C/G snv 2.0E-05 7.0E-05 2
rs147603016 0.925 0.160 5 177093286 synonymous variant G/A;C snv 1.5E-04; 8.2E-06 3
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
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
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12