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rs541862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs541862(A;G)
Make rs541862(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31949174
GeneCFB
is asnp
is mentioned by
dbSNPrs541862
ebirs541862
HLIrs541862
Exacrs541862
Varsomers541862
Maprs541862
PheGenIrs541862
hapmaprs541862
1000 genomesrs541862
hgdprs541862
ensemblrs541862
gopubmedrs541862
geneviewrs541862
scholarrs541862
googlers541862
pharmgkbrs541862
gwascentralrs541862
openSNPrs541862
23andMers541862
23andMe allrs541862
SNP Nexus

SNPshotrs541862
SNPdbers541862
MSV3drs541862
GWAS Ctlgrs541862
GMAF0.09963
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22694956OA-icon.png]
Trait
Title Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.
Risk Allele T
P-val 9E-17
Odds Ratio 1.8900 None


[PMID 22232432] Significance of C2/CFB variants in age-related macular degeneration and polypoidal choroidal vasculopathy in a Japanese population.