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: rs10118757
rs10118757
7 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 1.000 1 2009 2009
dbSNP: rs1017119
rs1017119
C5
1 1.000 0.080 9 121045260 intron variant T/C snv 2.0E-02 0.010 1.000 1 2016 2016
dbSNP: rs10204475
rs10204475
1 1.000 0.080 2 170076012 intron variant T/G snv 0.78 0.010 1.000 1 2010 2010
dbSNP: rs1042031
rs1042031
11 0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 0.010 1.000 1 2017 2017
dbSNP: rs1042579
rs1042579
16 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 0.010 1.000 1 2004 2004
dbSNP: rs10431036
rs10431036
1 1.000 0.080 11 112176338 5 prime UTR variant G/A snv 0.11 0.010 1.000 1 2019 2019
dbSNP: rs10435816
rs10435816
2 1.000 0.080 9 6225535 intron variant A/G snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs1044925
rs1044925
6 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 0.010 1.000 1 2014 2014
dbSNP: rs10487667
rs10487667
1 1.000 0.080 7 139984244 intron variant T/A;G snv 0.010 1.000 1 2018 2018
dbSNP: rs10489177
rs10489177
4 0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 0.010 1.000 1 2014 2014
dbSNP: rs1048943
rs1048943
88 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs1049255
rs1049255
9 0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 0.010 1.000 1 2011 2011
dbSNP: rs1051266
rs1051266
41 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 0.010 1.000 1 2015 2015
dbSNP: rs1051922
rs1051922
1 1.000 0.080 9 21077717 synonymous variant G/A snv 0.33 0.35 0.010 1.000 1 2020 2020
dbSNP: rs1051931
rs1051931
19 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 0.010 1.000 1 2014 2014
dbSNP: rs1057293
rs1057293
4 0.925 0.120 6 134172259 synonymous variant G/A snv 0.12 0.11 0.010 1.000 1 2011 2011
dbSNP: rs1057335
rs1057335
5 0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 0.010 1.000 1 2019 2019
dbSNP: rs1061170
rs1061170
CFH
72 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 < 0.001 1 2006 2006
dbSNP: rs1062708
rs1062708
1 1.000 0.080 19 49010016 missense variant C/A;G;T snv 4.3E-06; 1.7E-05; 0.48 0.010 1.000 1 2009 2009
dbSNP: rs1063537
rs1063537
6 0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 0.010 1.000 1 2018 2018
dbSNP: rs10719
rs10719
24 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 0.010 1.000 1 2018 2018
dbSNP: rs10741657
rs10741657
34 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 1.000 1 2018 2018
dbSNP: rs10754558
rs10754558
20 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 0.010 1.000 1 2016 2016
dbSNP: rs10759932
rs10759932
15 0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 0.010 1.000 1 2018 2018
dbSNP: rs10849373
rs10849373
1 1.000 0.080 12 631795 intron variant G/A snv 0.27 0.010 1.000 1 2011 2011