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rs11200014

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1.64x risk for breast cancer
(A;G) 1.20x risk for breast cancer
(G;G) common
ReferenceGRCh38 38.1/142
Chromosome10
Position121575416
GeneFGFR2
is asnp
is mentioned by
dbSNPrs11200014
ebirs11200014
HLIrs11200014
Exacrs11200014
Varsomers11200014
Maprs11200014
PheGenIrs11200014
hapmaprs11200014
1000 genomesrs11200014
hgdprs11200014
ensemblrs11200014
gopubmedrs11200014
geneviewrs11200014
scholarrs11200014
googlers11200014
pharmgkbrs11200014
gwascentralrs11200014
openSNPrs11200014
23andMers11200014
23andMe allrs11200014
SNP Nexus

SNPshotrs11200014
SNPdbers11200014
MSV3drs11200014
GWAS Ctlgrs11200014
GMAF0.3379
Max Magnitude
? (A;A) (A;G) (G;G) 28
This SNP is basically a proxy for SNP rs1219648, which represents the SNP in the FGFR2 gene with the strongest association with breast cancer. [PMID 17529973OA-icon.png]
Neighborrs7895676
Distance933
[PMID 18285324OA-icon.png] Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk.


[PMID 19223389OA-icon.png] FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation.


[PMID 19497954OA-icon.png] Histone-acetylated control of fibroblast growth factor receptor 2 intron 2 polymorphisms and isoform splicing in breast cancer.


[PMID 19500394OA-icon.png] Genetic variants in FGFR2 and FGFR4 genes and skin cancer risk in the Nurses' Health Study.


[PMID 20554749OA-icon.png] FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women.


[PMID 22965832] Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population.


[PMID 23124475] Three novel functional polymorphisms in the promoter of FGFR2 gene and breast cancer risk: a HuGE review and meta-analysis.