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: rs28938473
rs28938473
4 0.882 0.040 1 94007731 missense variant G/A snv 3.0E-03 3.6E-03 0.700 0
dbSNP: rs61750138
rs61750138
3 1.000 1 94030991 splice region variant C/A;T snv 1.2E-05 0.700 0
dbSNP: rs61751407
rs61751407
4 0.882 0.080 1 94010795 splice region variant C/A;T snv 3.1E-04 3.5E-04 0.700 0
dbSNP: rs61753033
rs61753033
4 0.882 0.080 1 94008767 missense variant A/G snv 2.0E-05 0.700 0
dbSNP: rs61753034
rs61753034
2 1.000 1 94007727 missense variant A/C snv 0.700 0
dbSNP: rs61751374
rs61751374
10 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 0.710 1.000 12 1997 2016
dbSNP: rs1800553
rs1800553
17 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 0.730 1.000 11 1997 2012
dbSNP: rs76157638
rs76157638
6 0.851 0.080 1 94051698 missense variant C/G;T snv 4.4E-03; 4.0E-06 0.720 1.000 8 1997 2014
dbSNP: rs61751408
rs61751408
5 0.851 0.080 1 94005509 missense variant G/A snv 2.0E-04 1.7E-04 0.700 1.000 6 1997 2014
dbSNP: rs61751392
rs61751392
7 0.827 0.080 1 94063250 missense variant A/G snv 1.5E-04 1.7E-04 0.700 1.000 19 1998 2017
dbSNP: rs61750200
rs61750200
8 0.790 0.080 1 94098928 missense variant G/A;T snv 1.1E-04; 8.0E-06 0.020 1.000 2 1998 1999
dbSNP: rs121909205
rs121909205
2 1.000 1 94120994 missense variant G/A;T snv 1.6E-05; 3.6E-05 0.010 1.000 1 1998 1998
dbSNP: rs150774447
rs150774447
2 1.000 1 94111579 missense variant C/A;T snv 4.0E-06; 2.4E-05 0.700 1.000 11 1999 2015
dbSNP: rs756840095
rs756840095
2 1.000 1 94042797 missense variant G/A snv 2.4E-05 6.3E-05 0.010 1.000 1 2002 2002
dbSNP: rs62645944
rs62645944
7 0.807 0.080 1 94098794 splice region variant C/A snv 8.8E-05 6.3E-05 0.010 1.000 1 2004 2004
dbSNP: rs61750120
rs61750120
4 0.882 0.160 1 94042767 missense variant G/A snv 1.2E-04 1.8E-04 0.010 1.000 1 2006 2006
dbSNP: rs760549861
rs760549861
2 1.000 1 94014685 missense variant G/A snv 7.6E-05 7.0E-06 0.710 1.000 6 2008 2018
dbSNP: rs121434491
rs121434491
15 0.752 0.200 2 55871091 missense variant G/A snv 0.010 1.000 1 2010 2010
dbSNP: rs137853300
rs137853300
2 1.000 0.040 22 32859277 missense variant C/G snv 0.010 1.000 1 2010 2010
dbSNP: rs3112831
rs3112831
2 1.000 0.080 1 94078678 missense variant T/C;G snv 0.26 0.26 0.010 1.000 1 2017 2017
dbSNP: rs1801466
rs1801466
3 1.000 1 94010911 missense variant T/A snv 4.3E-02 4.1E-02 0.030 1.000 3 2018 2019
dbSNP: rs1061170
rs1061170
CFH
72 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2018 2018
dbSNP: rs201471607
rs201471607
7 0.851 0.080 1 94046943 missense variant T/C snv 1.4E-04 7.7E-05 0.010 1.000 1 2018 2018
dbSNP: rs775179967
rs775179967
2 1.000 6 38791670 missense variant A/G snv 1.2E-05 1.4E-05 0.010 1.000 1 2018 2018