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: rs1764391
rs1764391
7 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 0.010 1.000 1 2010 2010
dbSNP: rs56302315
rs56302315
KDR
5 0.827 0.160 4 55089802 missense variant C/T snv 5.3E-04 4.1E-04 0.010 1.000 1 2015 2015
dbSNP: rs121913538
rs121913538
3 0.882 0.080 12 25245328 missense variant C/A;G snv 0.700 1.000 2 2014 2014
dbSNP: rs1206992207
rs1206992207
1 1.000 0.040 12 70587201 frameshift variant T/- del 0.010 1.000 1 2015 2015
dbSNP: rs121913529
rs121913529
144 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs180177133
rs180177133
9 0.807 0.240 16 23614089 frameshift variant T/- delins 1.2E-05 1.4E-05 0.700 0
dbSNP: rs760881374
rs760881374
1 1.000 0.040 19 35721464 missense variant G/A;T snv 1.6E-05 0.010 1.000 1 2014 2014