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: rs11154027
rs11154027
3 1.000 0.080 6 121460244 intergenic variant T/C snv 0.61 0.710 1.000 1 2019 2019
dbSNP: rs57224706
rs57224706
1 1.000 0.080 12 50086502 intron variant A/G snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs60713544
rs60713544
1 1.000 0.080 4 188193554 intergenic variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs12722
rs12722
6 0.882 0.120 9 134842570 3 prime UTR variant C/T snv 0.44 0.020 1.000 2 2009 2009
dbSNP: rs11225395
rs11225395
11 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs1144393
rs1144393
5 0.851 0.160 11 102798678 intron variant T/C snv 0.30 0.010 1.000 1 2016 2016
dbSNP: rs1799750
rs1799750
48 0.592 0.760 11 102799765 intron variant C/- delins 0.50 0.010 1.000 1 2016 2016
dbSNP: rs2252070
rs2252070
13 0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 0.010 1.000 1 2016 2016
dbSNP: rs2761884
rs2761884
3 0.925 0.120 14 53954334 intron variant G/T snv 0.34 0.010 1.000 1 2015 2015
dbSNP: rs3196378
rs3196378
4 0.882 0.080 9 134843036 3 prime UTR variant C/A;G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs4362400
rs4362400
2 1.000 0.080 16 77939459 intron variant A/C;G snv 0.49 0.010 1.000 1 2019 2019
dbSNP: rs587778430
rs587778430
KDR
7 0.807 0.280 4 55110466 missense variant C/T snv 1.2E-05 7.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs650108
rs650108
6 0.827 0.160 11 102838056 intron variant G/A snv 0.31 0.010 1.000 1 2009 2009
dbSNP: rs679620
rs679620
17 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 0.010 1.000 1 2009 2009
dbSNP: rs900379
rs900379
2 1.000 0.080 5 44369554 intron variant C/T snv 0.53 0.010 1.000 1 2015 2015
dbSNP: rs9505888
rs9505888
2 1.000 0.080 6 169225779 intron variant A/G snv 0.57 0.010 < 0.001 1 2014 2014