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: rs1130864
rs1130864
CRP
27 0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 0.010 1.000 1 2017 2017
dbSNP: rs1138272
rs1138272
GSTP1
42 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 0.010 < 0.001 1 2012 2012
dbSNP: rs1141718
rs1141718
SOD2
15 0.724 0.280 6 159688224 missense variant A/G snv 0.010 1.000 1 2010 2010
dbSNP: rs115333865
rs115333865
CGRRF1
1 1.000 0.040 14 54537731 missense variant G/A snv 1.9E-02 2.4E-02 0.010 1.000 1 2019 2019
dbSNP: rs115404146
rs115404146
HLA-C
1 1.000 0.040 6 31269031 3 prime UTR variant C/A;G snv 0.010 1.000 1 2017 2017
dbSNP: rs11542041
rs11542041
APOE
23 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.010 1.000 1 2006 2006
dbSNP: rs11549465
rs11549465
HIF1A ; HIF1A-AS3
55 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 0.010 1.000 1 2015 2015
dbSNP: rs11549467
rs11549467
HIF1A ; HIF1A-AS3
30 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 0.010 1.000 1 2015 2015
dbSNP: rs1155974
rs1155974
TNMD
2 0.925 0.120 X 100598284 intron variant C/T snv 0.34 0.010 1.000 1 2009 2009
dbSNP: rs11569536
rs11569536
C3
1 1.000 0.040 19 6686078 intron variant G/A snv 4.9E-02 6.1E-02 0.010 1.000 1 2015 2015
dbSNP: rs11603020
rs11603020
SERPING1
2 0.925 0.120 11 57606859 intron variant T/C snv 0.21 0.010 < 0.001 1 2010 2010
dbSNP: rs11671784
rs11671784
LOC284454 ; MIR23A ; MIR24-2 ; MIR27A
9 0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02 0.010 1.000 1 2019 2019
dbSNP: rs11715522
rs11715522
CX3CR1
1 1.000 0.040 3 39281672 missense variant A/C snv 0.42 0.35 0.010 1.000 1 2014 2014
dbSNP: rs117314762
rs117314762
CFB ; CYP21A2
1 1.000 0.040 6 31946529 missense variant G/A snv 7.7E-04 2.0E-04 0.010 1.000 1 2016 2016
dbSNP: rs1176281575
rs1176281575
SOD2
1 1.000 0.040 6 159684905 missense variant G/A snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs117793540
rs117793540
C3
2 0.925 0.040 19 6707118 missense variant G/A snv 2.2E-03 1.9E-03 0.010 1.000 1 2014 2014
dbSNP: rs1195312059
rs1195312059
ERG
3 0.882 0.040 21 38403680 missense variant G/A snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.010 1.000 1 2017 2017
dbSNP: rs12140421
rs12140421
CFHR3
1 1.000 0.040 1 196793654 3 prime UTR variant A/G snv 8.9E-03 0.010 1.000 1 2017 2017
dbSNP: rs121434303
rs121434303
FBLN5
3 0.882 0.120 14 91870336 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs121913058
rs121913058
CFH
2 0.925 0.200 1 196676018 missense variant G/A;C;T snv 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1239695899
rs1239695899
CFH
1 1.000 0.040 1 196673881 missense variant A/G snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs12636547
rs12636547
CX3CR1
1 1.000 0.040 3 39275337 intron variant G/C;T snv 0.010 1.000 1 2014 2014
dbSNP: rs12661281
rs12661281
CYP21A2 ; SLC44A4
3 0.882 0.040 6 31874821 missense variant T/A snv 0.15 0.11 0.010 1.000 1 2015 2015
dbSNP: rs12900948
rs12900948
RORA
1 1.000 0.040 15 61148472 intron variant C/A;T snv 0.010 1.000 1 2010 2010