Gene: CFH ×
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: rs10801555
rs10801555
CFH
1 1.000 0.040 1 196691131 intron variant A/G snv 0.64 0.800 1.000 4 2011 2013
dbSNP: rs10733086
rs10733086
CFH
1 1.000 0.040 1 196707805 intron variant A/C;T snv 0.800 1.000 3 2013 2018
dbSNP: rs2019727
rs2019727
CFH
1 1.000 0.040 1 196705584 intron variant T/A snv 0.24 0.700 1.000 3 2010 2013
dbSNP: rs203674
rs203674
CFH
1 1.000 0.040 1 196715495 intron variant G/T snv 0.65 0.710 1.000 3 2010 2015
dbSNP: rs551397
rs551397
CFH
1 1.000 0.040 1 196672942 intron variant C/T snv 0.31 0.40 0.030 1.000 3 2008 2018
dbSNP: rs6428357
rs6428357
CFH
1 1.000 0.040 1 196706441 intron variant A/G snv 0.62 0.700 1.000 3 2011 2013
dbSNP: rs1061147
rs1061147
CFH
1 1.000 0.040 1 196685194 synonymous variant A/C snv 0.68 0.62 0.810 1.000 2 2007 2013
dbSNP: rs1329424
rs1329424
CFH
1 1.000 0.040 1 196677046 non coding transcript exon variant T/G snv 0.66 0.800 1.000 2 2010 2013
dbSNP: rs2019724
rs2019724
CFH
1 1.000 0.040 1 196705787 intron variant T/C snv 0.62 0.700 1.000 2 2011 2013
dbSNP: rs203687
rs203687
CFH
1 1.000 0.040 1 196705140 intron variant C/T snv 0.71 0.700 1.000 2 2013 2013
dbSNP: rs395544
rs395544
CFH
1 1.000 0.040 1 196729142 intron variant A/G;T snv 0.700 1.000 2 2013 2013
dbSNP: rs403846
rs403846
CFH
1 1.000 0.040 1 196727607 intron variant T/C snv 0.67 0.700 1.000 2 2013 2013
dbSNP: rs424535
rs424535
CFH
1 1.000 0.040 1 196740093 intron variant A/T snv 0.48 0.700 1.000 2 2013 2013
dbSNP: rs7529589
rs7529589
CFH
1 1.000 0.040 1 196689149 intron variant T/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs10801554
rs10801554
CFH
1 1.000 0.040 1 196688525 intron variant C/T snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs10801556
rs10801556
CFH
1 1.000 0.040 1 196691334 intron variant A/G snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs10922094
rs10922094
CFH
1 1.000 0.040 1 196692375 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10922096
rs10922096
CFH
1 1.000 0.040 1 196693329 intron variant T/C snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs10922102
rs10922102
CFH
1 1.000 0.040 1 196699157 intron variant C/T snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs12045503
rs12045503
CFH
1 1.000 0.040 1 196703343 intron variant C/T snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs12127759
rs12127759
CFH
1 1.000 0.040 1 196679483 non coding transcript exon variant C/A;T snv 0.700 1.000 1 2013 2013
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: rs1329421
rs1329421
CFH
1 1.000 0.040 1 196687075 intron variant A/T snv 0.62 0.700 1.000 1 2013 2013
dbSNP: rs1329422
rs1329422
CFH
1 1.000 0.040 1 196686150 intron variant C/G snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs139360826
rs139360826
CFH
1 1.000 0.040 1 196677572 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2017 2017