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: rs1267969615
rs1267969615
ACE
100 0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs1302207706
rs1302207706
PON1
2 1.000 0.080 7 95316748 missense variant C/T snv 0.010 1.000 1 2009 2009
dbSNP: rs1365501228
rs1365501228
VEGFA
2 1.000 0.080 6 43770732 missense variant C/T snv 1.4E-05 0.010 1.000 1 2009 2009
dbSNP: rs1695
rs1695
GSTP1
188 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2009 2009
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.010 1.000 1 2005 2005
dbSNP: rs1799983
rs1799983
NOS3
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2005 2005
dbSNP: rs370402227
rs370402227
NOS3
4 0.925 0.120 7 150996443 missense variant G/A;C snv 1.1E-05 0.010 1.000 1 2009 2009
dbSNP: rs45539933
rs45539933
UCP1
5 0.882 0.280 4 140567914 missense variant C/T snv 8.7E-02 7.7E-02 0.010 1.000 1 2009 2009
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2006 2006
dbSNP: rs771561387
rs771561387
VEGFA
2 1.000 0.080 6 43784557 missense variant C/G;T snv 4.0E-06; 1.2E-05 0.010 < 0.001 1 2009 2009
dbSNP: rs953038635
rs953038635
SOD2
51 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 0.010 1.000 1 2009 2009