Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121913499
rs121913499
34 0.630 0.464 2 208248389 missense variant G/A,C,T snp 0.720 1.000 4 2009 2015
dbSNP: rs121913503
rs121913503
17 0.724 0.179 15 90088606 missense variant C/A,T snp 0.700 2 2009 2016
dbSNP: rs2297440
rs2297440
5 0.821 0.071 20 63680946 intron variant T/C snp 0.80 0.020 1.000 2 2014 2015
dbSNP: rs10464870
rs10464870
3 0.878 0.071 8 129465577 intron variant C/T snp 0.79 0.010 1.000 1 2015 2015
dbSNP: rs1057519898
rs1057519898
5 0.846 0.107 8 38417333 missense variant T/C snp 0.700 1 2016 2016
dbSNP: rs1057519899
rs1057519899
5 0.846 0.107 8 38417879 missense variant T/C snp 0.700 1 2016 2016
dbSNP: rs1057519903
rs1057519903
2 0.923 0.071 1 226064434 missense variant A/T snp 0.700 1 2016 2016
dbSNP: rs121918464
rs121918464
15 0.756 0.321 12 112450406 missense variant G/A,C snp 0.700 1 2016 2016
dbSNP: rs121918465
rs121918465
7 0.821 0.179 12 112450407 missense variant A/C,G,T snp 0.700 1 2016 2016
dbSNP: rs2071559
rs2071559
KDR
6 0.846 0.179 4 55126199 regulatory region variant A/G snp 0.52 0.010 1.000 1 2016 2016
dbSNP: rs281865545
rs281865545
7 0.784 0.214 17 64377836 missense variant C/G,T snp 0.010 1.000 1 2009 2009
dbSNP: rs2853676
rs2853676
15 0.724 0.214 5 1288432 intron variant T/A,C snp 0.76 0.010 1.000 1 2014 2014
dbSNP: rs28933368
rs28933368
7 0.801 0.071 17 39725721 missense variant G/A snp 0.700 1 2004 2004
dbSNP: rs4809324
rs4809324
3 0.923 0.071 20 63686867 non coding transcript exon variant T/C snp 8.2E-02 0.010 1.000 1 2015 2015
dbSNP: rs55832599
rs55832599
3 0.923 0.071 17 7673821 missense variant G/A snp 0.010 1.000 1 2002 2002
dbSNP: rs58064122
rs58064122
2 0.923 0.143 17 44913334 missense variant G/A,C snp 0.010 1.000 1 2012 2012
dbSNP: rs6010620
rs6010620
11 0.769 0.250 20 63678486 intron variant A/C,G snp 0.80 0.010 1.000 1 2014 2014
dbSNP: rs6089953
rs6089953
1 1.000 0.036 20 63659655 intron variant A/G snp 0.81 0.010 1.000 1 2015 2015
dbSNP: rs71305152
rs71305152
2 0.923 0.036 8 105437494 intron variant A/ATTTTCT in-del 3.2E-05; 0.42 0.010 1.000 1 2016 2016
dbSNP: rs765848205
rs765848205
15 0.734 0.214 17 7674253 missense variant A/C,T snp 0.010 1.000 1 2014 2014
dbSNP: rs868162712
rs868162712
2 1.000 0.036 18 55279598 missense variant G/A snp 0.010 1.000 1 2002 2002
dbSNP: rs869320694
rs869320694
7 0.784 0.393 8 38414790 missense variant T/C snp 0.700 1 2016 2016
dbSNP: rs891835
rs891835
4 0.878 0.071 8 129479506 intron variant T/G snp 0.19 0.010 1.000 1 2015 2015
dbSNP: rs1801516
rs1801516
ATM
15 0.715 0.214 11 108304735 missense variant G/A snp 0.11 0.11 0.010 1.000 1 2009 2009
dbSNP: rs770374782
rs770374782
3 0.878 0.143 17 7673752 missense variant G/A snp 1.2E-05 3.2E-05 0.010 1.000 1 2009 2009