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: rs7535263
rs7535263
CFH
3 0.925 0.080 1 196713216 intron variant G/A;C snv 0.010 1.000 1 2010 2010
dbSNP: rs10754199
rs10754199
CFH
2 1.000 0.040 1 196701709 intron variant A/G snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs976333015
rs976333015
CFH
3 0.882 0.200 1 196673077 missense variant G/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs10737680
rs10737680
CFH
9 0.827 0.080 1 196710325 intron variant A/C snv 0.44 0.800 1.000 4 2010 2013
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: rs380390
rs380390
CFH
2 0.925 0.160 1 196731921 intron variant G/A;C;T snv 0.810 1.000 4 2005 2013
dbSNP: rs572515
rs572515
CFH
2 0.925 0.160 1 196677131 non coding transcript exon variant A/G;T snv 0.710 1.000 4 2008 2013
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: rs393955
rs393955
CFH
2 0.925 0.040 1 196723340 intron variant C/A snv 0.65 0.720 1.000 3 2012 2013
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: rs6677604
rs6677604
CFH
7 0.827 0.200 1 196717788 intron variant G/A snv 0.23 0.720 1.000 3 2013 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: rs10801553
rs10801553
CFH
2 1.000 0.040 1 196686613 intron variant A/C snv 0.64 0.700 1.000 2 2013 2013
dbSNP: rs12038333
rs12038333
CFH
2 1.000 0.040 1 196703324 intron variant G/A snv 0.64 0.700 1.000 2 2010 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: rs1831282
rs1831282
CFH
2 1.000 0.040 1 196704863 intron variant A/C snv 0.62 0.800 1.000 2 2013 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: rs379489
rs379489
CFH
4 0.851 0.200 1 196724321 intron variant A/G snv 0.65 0.700 1.000 2 2011 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: rs6695321
rs6695321
CFH
2 1.000 0.040 1 196706731 intron variant A/G snv 0.36 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