Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs17251221 0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs6259 0.658 0.400 17 7633209 missense variant G/A snv 8.9E-02 8.1E-02 27
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35