Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs6259 0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 27
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs10046 0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs6166 0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 17
rs6165 0.724 0.160 2 48963902 missense variant C/G;T snv 4.0E-06; 0.55 14
rs10895068 0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs121909658 0.776 0.200 2 48983125 missense variant G/A snv 6.9E-04 5.8E-04 8
rs184752888 0.882 0.120 6 32977847 missense variant G/A snv 4
rs2293275 0.851 0.160 2 48694236 missense variant T/C snv 0.61 0.51 4
rs386833511 0.882 0.200 2 48963097 missense variant G/A snv 3
rs1440086679 0.925 0.120 6 32979854 missense variant C/T snv 4.1E-06 2
rs121909659 0.925 0.160 2 48989022 missense variant A/G;T snv 4.0E-05; 4.0E-06 2
rs121909665 0.925 0.160 2 48990629 missense variant G/T snv 2
rs41308602 1.000 0.080 X 50911091 missense variant A/G snv 5.7E-02 5.1E-02 1
rs121909663 1.000 0.080 2 48963476 missense variant T/C snv 1
rs121909664 1.000 0.080 2 48963187 missense variant A/G;T snv 4.0E-06; 4.0E-06 1
rs28928870 1.000 0.080 2 48963475 missense variant G/A;T snv 4.0E-06 1
rs28928871 1.000 0.080 2 48963122 missense variant C/T snv 1
rs1870378
KDR
1.000 0.080 4 55100286 intron variant C/T snv 0.21 1
rs2305945
KDR
1.000 0.080 4 55105679 intron variant G/T snv 0.35 1
rs4073366 1.000 0.080 2 48755483 intron variant C/G snv 0.19 0.16 1