Have questions? Visit https://www.reddit.com/r/SNPedia

rs1473307

From SNPedia

Orientationplus
Stabilizedplus
Make rs1473307(C;C)
Make rs1473307(C;T)
Make rs1473307(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position225360907
is asnp
is mentioned by
dbSNPrs1473307
dbSNP (classic)rs1473307
ClinGenrs1473307
ebirs1473307
HLIrs1473307
Exacrs1473307
Gnomadrs1473307
Varsomers1473307
LitVarrs1473307
Maprs1473307
PheGenIrs1473307
Biobankrs1473307
1000 genomesrs1473307
hgdprs1473307
ensemblrs1473307
geneviewrs1473307
scholarrs1473307
googlers1473307
pharmgkbrs1473307
gwascentralrs1473307
openSNPrs1473307
23andMers1473307
SNPshotrs1473307
SNPdbers1473307
MSV3drs1473307
GWAS Ctlgrs1473307
GMAF0.4169
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23307926OA-icon.png]
Trait Menopause (age at onset)
Title A genome-wide association study of early menopause and the combined impact of identified variants.
Risk Allele T
P-val 3E-7
Odds Ratio .14 [0.089-0.199] years decrease