Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs3869109 0.851 0.160 6 31216419 intergenic variant A/G;T snv 5
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs17757541 0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs6136 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs3819025 0.752 0.480 6 52186476 intron variant G/A snv 0.13 8.5E-02 11
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111