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: rs1870378
rs1870378
KDR
1 1.000 0.080 4 55100286 intron variant C/T snv 0.21 0.010 1.000 1 2014 2014
dbSNP: rs2305945
rs2305945
KDR
1 1.000 0.080 4 55105679 intron variant G/T snv 0.35 0.010 1.000 1 2014 2014
dbSNP: rs2305948
rs2305948
KDR
18 0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 0.010 1.000 1 2014 2014