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rs7524776

From SNPedia

Orientationplus
Stabilizedplus
Make rs7524776(C;C)
Make rs7524776(C;T)
Make rs7524776(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position196654207
GeneCFH
is asnp
is mentioned by
dbSNPrs7524776
ebirs7524776
HLIrs7524776
Exacrs7524776
Varsomers7524776
Maprs7524776
PheGenIrs7524776
hapmaprs7524776
1000 genomesrs7524776
hgdprs7524776
ensemblrs7524776
gopubmedrs7524776
geneviewrs7524776
scholarrs7524776
googlers7524776
pharmgkbrs7524776
gwascentralrs7524776
openSNPrs7524776
23andMers7524776
23andMe allrs7524776
SNP Nexus

SNPshotrs7524776
SNPdbers7524776
MSV3drs7524776
GWAS Ctlgrs7524776
GMAF0.118
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21882633] [Influence of genetic mutations on clinical presentation of subretinal neovascularization. Report 1: The impact of CFH and IL-8 genes polymorphism]