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rs4698775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4698775(G;T)
Make rs4698775(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position109669323
GeneCCDC109B
is asnp
is mentioned by
dbSNPrs4698775
ebirs4698775
HLIrs4698775
Exacrs4698775
Varsomers4698775
Maprs4698775
PheGenIrs4698775
hapmaprs4698775
1000 genomesrs4698775
hgdprs4698775
ensemblrs4698775
gopubmedrs4698775
geneviewrs4698775
scholarrs4698775
googlers4698775
pharmgkbrs4698775
gwascentralrs4698775
openSNPrs4698775
23andMers4698775
23andMe allrs4698775
SNP Nexus

SNPshotrs4698775
SNPdbers4698775
MSV3drs4698775
GWAS Ctlgrs4698775
GMAF0.2241
Max Magnitude0
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23455636OA-icon.png]
Trait Age-related macular degeneration
Title Seven new loci associated with age-related macular degeneration.
Risk Allele G
P-val 7E-11
Odds Ratio 1.14 [1.10-1.17]


ClinVar
Risk rs4698775(T;T)
Alt rs4698775(T;T)
Reference rs4698775(G;G)
Significance Untested
Disease not provided
Variation info
Gene CCDC109B
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.110590479G>T
CLNSRC
CLNACC RCV000190300.1,