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rs514943

From SNPedia

Orientationminus
Stabilizedminus
Make rs514943(A;A)
Make rs514943(A;G)
Make rs514943(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position196694783
GeneCFH
is asnp
is mentioned by
dbSNPrs514943
ebirs514943
HLIrs514943
Exacrs514943
Varsomers514943
Maprs514943
PheGenIrs514943
hapmaprs514943
1000 genomesrs514943
hgdprs514943
ensemblrs514943
gopubmedrs514943
geneviewrs514943
scholarrs514943
googlers514943
pharmgkbrs514943
gwascentralrs514943
openSNPrs514943
23andMers514943
23andMe allrs514943
SNP Nexus

SNPshotrs514943
SNPdbers514943
MSV3drs514943
GWAS Ctlgrs514943
GMAF0.2342
Max Magnitude
? (A;A) (A;G) (G;G) 28

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


[PMID 16936733OA-icon.png] CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.