Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2200733 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 12
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs1126643 0.807 0.160 5 53051539 synonymous variant C/T snv 0.39 0.36 6
rs12522248 0.925 0.080 5 157052415 missense variant T/C snv 0.29 0.26 2
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs6882076 0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
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
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs5985 0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31