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rs2947411

From SNPedia

Orientationminus
Stabilizedminus
Make rs2947411(C;C)
Make rs2947411(C;T)
Make rs2947411(T;T)
ReferenceGRCh37 37.1/132
Chromosome2
Position614168
is asnp
is mentioned by
dbSNPrs2947411
dbSNP (classic)rs2947411
ClinGenrs2947411
ebirs2947411
HLIrs2947411
Exacrs2947411
Gnomadrs2947411
Varsomers2947411
LitVarrs2947411
Maprs2947411
PheGenIrs2947411
Biobankrs2947411
1000 genomesrs2947411
hgdprs2947411
ensemblrs2947411
geneviewrs2947411
scholarrs2947411
googlers2947411
pharmgkbrs2947411
gwascentralrs2947411
openSNPrs2947411
23andMers2947411
SNPshotrs2947411
SNPdbers2947411
MSV3drs2947411
GWAS Ctlgrs2947411
GMAF0.1662
Max Magnitude0
? (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 A
P-val 2E-8
Odds Ratio 2.8000 [1.82-3.78] week increase


[PMID 29073238OA-icon.png] Genetic variations, reproductive aging, and breast cancer risk in African American and European American women: The Women's Circle of Health Study.