Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1443292790 1.000 0.120 17 63929438 missense variant T/C snv 2
rs6773854 1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 2
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs140522 0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs6773363 1.000 0.120 3 27752141 intergenic variant T/A;C snv 1
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2523607 1.000 0.120 6 31355013 non coding transcript exon variant T/A snv 1
rs7712513 0.925 0.120 5 122582513 intergenic variant G/T snv 0.71 2
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 27
rs121913238 0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs79464052 1.000 0.120 5 141655607 intron variant G/C snv 7.1E-02 7.8E-02 1
rs2279115 0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs1801195
WRN
0.776 0.240 8 31141764 missense variant G/A;T snv 8.0E-06; 0.45 0.46 8
rs1312391542 0.925 0.120 6 106104897 missense variant G/A;T snv 2
rs35090414 0.925 0.120 11 45224227 missense variant G/A;T snv 1.5E-04; 8.2E-02 2
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 31