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rs11878133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11878133(C;C)
Make rs11878133(C;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position60399804
is asnp
is mentioned by
dbSNPrs11878133
ebirs11878133
HLIrs11878133
Exacrs11878133
Varsomers11878133
Maprs11878133
PheGenIrs11878133
hapmaprs11878133
1000 genomesrs11878133
hgdprs11878133
ensemblrs11878133
gopubmedrs11878133
geneviewrs11878133
scholarrs11878133
googlers11878133
pharmgkbrs11878133
gwascentralrs11878133
openSNPrs11878133
23andMers11878133
23andMe allrs11878133
SNP Nexus

SNPshotrs11878133
SNPdbers11878133
MSV3drs11878133
GWAS Ctlgrs11878133
GMAF0.03857
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20385819OA-icon.png]
Trait Age-related macular degeneration
Title Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
Risk Allele T
P-val 0.000004
Odds Ratio None None