rs9920722
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9920722(C;C) |
Make rs9920722(C;T) |
Make rs9920722(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 49442915 |
Gene | FAM227B, FGF7 |
is a | snp |
is | mentioned by |
dbSNP | rs9920722 |
dbSNP (classic) | rs9920722 |
ClinGen | rs9920722 |
ebi | rs9920722 |
HLI | rs9920722 |
Exac | rs9920722 |
Gnomad | rs9920722 |
Varsome | rs9920722 |
LitVar | rs9920722 |
Map | rs9920722 |
PheGenI | rs9920722 |
Biobank | rs9920722 |
1000 genomes | rs9920722 |
hgdp | rs9920722 |
ensembl | rs9920722 |
geneview | rs9920722 |
scholar | rs9920722 |
rs9920722 | |
pharmgkb | rs9920722 |
gwascentral | rs9920722 |
openSNP | rs9920722 |
23andMe | rs9920722 |
SNPshot | rs9920722 |
SNPdbe | rs9920722 |
MSV3d | rs9920722 |
GWAS Ctlg | rs9920722 |
GMAF | 0.3356 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24146310] Genetic Variants in the Fibroblast Growth Factor Pathway as Potential Markers of Ovarian Cancer Risk, Therapeutic Response, and Clinical Outcome