Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs9797861 0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs17568 0.752 0.320 1 1212042 synonymous variant C/T snv 0.37 0.31 12
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35