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rs4849887

From SNPedia

Orientationplus
Stabilizedplus
Make rs4849887(C;C)
Make rs4849887(C;T)
Make rs4849887(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position120487546
is asnp
is mentioned by
dbSNPrs4849887
ebirs4849887
HLIrs4849887
Exacrs4849887
Varsomers4849887
Maprs4849887
PheGenIrs4849887
hapmaprs4849887
1000 genomesrs4849887
hgdprs4849887
ensemblrs4849887
gopubmedrs4849887
geneviewrs4849887
scholarrs4849887
googlers4849887
pharmgkbrs4849887
gwascentralrs4849887
openSNPrs4849887
23andMers4849887
23andMe allrs4849887
SNP Nexus

SNPshotrs4849887
SNPdbers4849887
MSV3drs4849887
GWAS Ctlgrs4849887
GMAF0.1639
Max Magnitude
? (C;C) (C;T) (T;T) 28
breast size

[PMID 22747683OA-icon.png] Genetic variants associated with breast size also influence breast cancer risk

GWAS snp
PMID [PMID 23535729OA-icon.png]
Trait Breast cancer
Title Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
Risk Allele C
P-val 4E-11
Odds Ratio 1.10 [1.06-1.14]


[PMID 25007960] Association study of susceptibility loci with specific breast cancer subtypes in Chinese women