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rs9920722

From SNPedia

Orientationplus
Stabilizedplus
Make rs9920722(C;C)
Make rs9920722(C;T)
Make rs9920722(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position49442915
GeneFAM227B, FGF7
is asnp
is mentioned by
dbSNPrs9920722
ebirs9920722
HLIrs9920722
Exacrs9920722
Varsomers9920722
Maprs9920722
PheGenIrs9920722
hapmaprs9920722
1000 genomesrs9920722
hgdprs9920722
ensemblrs9920722
gopubmedrs9920722
geneviewrs9920722
scholarrs9920722
googlers9920722
pharmgkbrs9920722
gwascentralrs9920722
openSNPrs9920722
23andMers9920722
23andMe allrs9920722
SNP Nexus

SNPshotrs9920722
SNPdbers9920722
MSV3drs9920722
GWAS Ctlgrs9920722
GMAF0.3356
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24146310OA-icon.png] Genetic Variants in the Fibroblast Growth Factor Pathway as Potential Markers of Ovarian Cancer Risk, Therapeutic Response, and Clinical Outcome