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rs17102287

From SNPedia

Orientationplus
Stabilizedplus
Make rs17102287(C;C)
Make rs17102287(C;T)
Make rs17102287(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position121590677
GeneFGFR2
is asnp
is mentioned by
dbSNPrs17102287
ebirs17102287
HLIrs17102287
Exacrs17102287
Varsomers17102287
Maprs17102287
PheGenIrs17102287
hapmaprs17102287
1000 genomesrs17102287
hgdprs17102287
ensemblrs17102287
gopubmedrs17102287
geneviewrs17102287
scholarrs17102287
googlers17102287
pharmgkbrs17102287
gwascentralrs17102287
openSNPrs17102287
23andMers17102287
23andMe allrs17102287
SNP Nexus

SNPshotrs17102287
SNPdbers17102287
MSV3drs17102287
GWAS Ctlgrs17102287
GMAF0.2236
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21822685] Genetic variants of fibroblast growth factor receptor 2 (FGFR2) are associated with breast cancer risk in Chinese women of the Han nationality


[PMID 18285324OA-icon.png] Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk.