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: rs193922219
rs193922219
7 0.784 0.214 15 48446701 splice region variant C/A,T snp 0.700 0
dbSNP: rs662
rs662
71 0.561 0.607 7 95308134 missense variant T/C snp 0.38 0.41 0.050 1.000 5 2000 2017
dbSNP: rs854560
rs854560
51 0.599 0.500 7 95316772 missense variant A/C,G,N,T snp 0.29 0.29 0.040 1.000 4 2000 2017
dbSNP: rs7493
rs7493
23 0.679 0.357 7 95405463 missense variant G/C snp 0.27 0.28 0.030 1.000 3 2000 2017
dbSNP: rs3024477
rs3024477
2 0.923 0.071 6 6250887 missense variant T/A snp 1.8E-02 2.1E-02 0.020 1.000 2 2002 2008
dbSNP: rs5982
rs5982
2 0.923 0.071 6 6174633 missense variant G/A snp 0.21 0.19 0.010 1.000 1 2002 2002
dbSNP: rs5985
rs5985
12 0.734 0.214 6 6318562 missense variant C/A,T snp 0.20; 2.4E-05 0.22 0.010 1.000 1 2002 2002
dbSNP: rs201058276
rs201058276
F7
17 0.724 0.214 13 113118731 missense variant G/A,C snp 4.8E-05; 4.0E-06 9.6E-05 0.020 < 0.001 2 2003 2008
dbSNP: rs5498
rs5498
53 0.570 0.679 19 10285007 missense variant A/G snp 0.44 0.36 0.010 1.000 1 2003 2003
dbSNP: rs1654413
rs1654413
1 1.000 0.071 19 55014991 missense variant A/G,T snp 3.7E-05; 2.0E-05; 0.80; 4.4E-04 3.2E-05; 3.2E-05; 3.2E-05; 0.76; 1.5E-03 0.010 1.000 1 2004 2004
dbSNP: rs1799983
rs1799983
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.090 1.000 9 2005 2014
dbSNP: rs1801133
rs1801133
86 0.533 0.714 1 11796321 missense variant G/A snp 0.31 0.26 0.040 0.750 4 2005 2015
dbSNP: rs4986790
rs4986790
146 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.010 < 0.001 1 2005 2005
dbSNP: rs5443
rs5443
65 0.570 0.571 12 6845711 synonymous variant C/T snp 0.36 0.43 0.010 1.000 1 2005 2005
dbSNP: rs751377893
rs751377893
F5
26 0.652 0.464 1 169546513 missense variant T/C snp 4.0E-06 0.010 < 0.001 1 2005 2005
dbSNP: rs375752214
rs375752214
13 0.756 0.214 7 150998541 missense variant C/T snp 4.1E-06 3.2E-05 0.050 1.000 5 2006 2018
dbSNP: rs1061170
rs1061170
CFH
53 0.575 0.607 1 196690107 missense variant C/T snp 0.68 0.63 0.020 0.500 2 2006 2008
dbSNP: rs1800947
rs1800947
CRP
14 0.734 0.250 1 159713648 splice region variant C/A,G,T snp 4.4E-05; 5.1E-02; 4.0E-06 3.2E-05; 5.0E-02 0.020 1.000 2 2006 2014
dbSNP: rs966221
rs966221
2 1.000 0.071 5 60206693 intron variant A/G snp 0.56 0.020 1.000 2 2006 2014
dbSNP: rs1205
rs1205
CRP
30 0.652 0.500 1 159712443 3 prime UTR variant C/T snp 0.32 0.010 1.000 1 2006 2006
dbSNP: rs1341665
rs1341665
3 1.000 0.071 1 159721769 intergenic variant G/A snp 0.33 0.010 1.000 1 2006 2006
dbSNP: rs1501299
rs1501299
28 0.647 0.536 3 186853334 intron variant G/C,T snp 6.4E-05; 0.30 0.010 < 0.001 1 2006 2006
dbSNP: rs1800470
rs1800470
46 0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60 0.010 1.000 1 2006 2006
dbSNP: rs182052
rs182052
9 0.801 0.250 3 186842993 intron variant G/A snp 0.39 0.010 1.000 1 2006 2006
dbSNP: rs266729
rs266729
21 0.679 0.429 3 186841685 intergenic variant C/A,G,T snp 6.4E-05; 0.23 0.010 1.000 1 2006 2006