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rs4929923

From SNPedia

Orientationplus
Stabilizedplus
Make rs4929923(C;C)
Make rs4929923(C;T)
Make rs4929923(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position8617653
GeneTRIM66
is asnp
is mentioned by
dbSNPrs4929923
ebirs4929923
HLIrs4929923
Exacrs4929923
Varsomers4929923
Maprs4929923
PheGenIrs4929923
hapmaprs4929923
1000 genomesrs4929923
hgdprs4929923
ensemblrs4929923
gopubmedrs4929923
geneviewrs4929923
scholarrs4929923
googlers4929923
pharmgkbrs4929923
gwascentralrs4929923
openSNPrs4929923
23andMers4929923
23andMe allrs4929923
SNP Nexus

SNPshotrs4929923
SNPdbers4929923
MSV3drs4929923
GWAS Ctlgrs4929923
GMAF0.4591
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21102462OA-icon.png]
Trait
Title Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Risk Allele T
P-val 1E-8
Odds Ratio 2.3000 [1.52-3.08] week increase