Source: ALL
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: rs1549758
rs1549758
NOS3
7 0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 0.010 1.000 1 2019 2019
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 2019 2019
dbSNP: rs5754312
rs5754312
TIMP3 ; SYN3
1 22 32848434 intron variant A/T snv 0.52 0.010 1.000 1 2019 2019
dbSNP: rs708269
rs708269
MMP2
1 16 55481783 5 prime UTR variant A/T snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs715572
rs715572
TIMP3 ; SYN3
3 0.925 0.040 22 32838944 intron variant G/A snv 0.18 0.010 1.000 1 2019 2019
dbSNP: rs7667298
rs7667298
KDR
7 0.827 0.120 4 55125564 5 prime UTR variant T/C snv 0.48 0.010 1.000 1 2019 2019
dbSNP: rs9766678
rs9766678
THBS2 ; LOC101929523
1 6 169237816 intron variant G/A snv 0.61 0.61 0.010 1.000 1 2019 2019