rs17542768
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17542768(A;A) |
Make rs17542768(A;G) |
Make rs17542768(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 121578300 |
Gene | FGFR2 |
is a | snp |
is | mentioned by |
dbSNP | rs17542768 |
dbSNP (classic) | rs17542768 |
ClinGen | rs17542768 |
ebi | rs17542768 |
HLI | rs17542768 |
Exac | rs17542768 |
Gnomad | rs17542768 |
Varsome | rs17542768 |
LitVar | rs17542768 |
Map | rs17542768 |
PheGenI | rs17542768 |
Biobank | rs17542768 |
1000 genomes | rs17542768 |
hgdp | rs17542768 |
ensembl | rs17542768 |
geneview | rs17542768 |
scholar | rs17542768 |
rs17542768 | |
pharmgkb | rs17542768 |
gwascentral | rs17542768 |
openSNP | rs17542768 |
23andMe | rs17542768 |
SNPshot | rs17542768 |
SNPdbe | rs17542768 |
MSV3d | rs17542768 |
GWAS Ctlg | rs17542768 |
GMAF | 0.09963 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 18285324] Common variation in the fibroblast growth factor receptor 2 gene is not associated with endometriosis risk.