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: rs10019009
rs10019009
4 0.851 0.080 4 87661983 missense variant A/G;T snv 4.0E-06; 0.29 0.010 1.000 1 2016 2016
dbSNP: rs1004189
rs1004189
1 1.000 0.040 2 208349547 intron variant T/G snv 0.010 1.000 1 2009 2009
dbSNP: rs10065172
rs10065172
8 0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 0.010 < 0.001 1 2017 2017
dbSNP: rs1009759
rs1009759
1 1.000 0.040 9 5556786 intron variant A/C;G snv 0.010 < 0.001 1 2011 2011
dbSNP: rs10204525
rs10204525
20 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 0.010 1.000 1 2019 2019
dbSNP: rs10208769
rs10208769
1 1.000 0.040 2 61378479 intron variant T/A snv 0.48 0.010 1.000 1 2017 2017
dbSNP: rs1024446168
rs1024446168
1 1.000 0.040 X 47583421 synonymous variant C/A snv 1.7E-05 0.010 1.000 1 2009 2009
dbSNP: rs1045642
rs1045642
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 < 0.001 1 2017 2017
dbSNP: rs1048274
rs1048274
1 1.000 0.040 9 6256292 3 prime UTR variant G/A snv 0.35 0.010 1.000 1 2014 2014
dbSNP: rs10489630
rs10489630
2 0.925 0.040 1 67196939 intron variant A/C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10494829
rs10494829
1 1.000 0.040 1 200968901 downstream gene variant G/A snv 0.26 0.010 1.000 1 2013 2013
dbSNP: rs10499194
rs10499194
10 0.752 0.400 6 137681500 intron variant C/T snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs1050501
rs1050501
15 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 0.010 < 0.001 1 2012 2012
dbSNP: rs1053005
rs1053005
10 0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 0.010 1.000 1 2011 2011
dbSNP: rs1055234
rs1055234
1 1.000 0.040 19 54154264 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2012 2012
dbSNP: rs1056836
rs1056836
58 0.581 0.680 2 38071060 missense variant G/C snv 0.51 0.010 1.000 1 2019 2019
dbSNP: rs1061622
rs1061622
33 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2018 2018
dbSNP: rs1061680
rs1061680
2 1.000 0.040 19 54632001 missense variant C/T snv 0.010 < 0.001 1 2019 2019
dbSNP: rs1065489
rs1065489
CFH
19 0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 0.010 1.000 1 2016 2016
dbSNP: rs1077667
rs1077667
2 0.925 0.120 19 6668961 intron variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs10917661
rs10917661
3 0.882 0.160 1 161671427 stop gained C/T snv 2.8E-05 0.010 < 0.001 1 2012 2012
dbSNP: rs11062357
rs11062357
1 1.000 0.040 12 312228 intron variant T/C snv 0.33 0.010 1.000 1 2013 2013
dbSNP: rs11062385
rs11062385
1 1.000 0.040 12 318409 missense variant A/C;G snv 1.2E-05; 0.31 0.010 1.000 1 2011 2011
dbSNP: rs11145835
rs11145835
1 1.000 0.040 9 136390000 intron variant A/G snv 0.10 0.010 1.000 1 2014 2014
dbSNP: rs11187265
rs11187265
1 1.000 0.040 10 93064409 missense variant G/A snv 0.10 8.8E-02 0.010 < 0.001 1 2007 2007