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rs10760502

From SNPedia

Orientationplus
Stabilizedplus
Make rs10760502(A;A)
Make rs10760502(A;G)
Make rs10760502(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position127802988
GeneFPGS
is asnp
is mentioned by
dbSNPrs10760502
ebirs10760502
HLIrs10760502
Exacrs10760502
Varsomers10760502
Maprs10760502
PheGenIrs10760502
hapmaprs10760502
1000 genomesrs10760502
hgdprs10760502
ensemblrs10760502
gopubmedrs10760502
geneviewrs10760502
scholarrs10760502
googlers10760502
pharmgkbrs10760502
gwascentralrs10760502
openSNPrs10760502
23andMers10760502
23andMe allrs10760502
SNP Nexus

SNPshotrs10760502
SNPdbers10760502
MSV3drs10760502
GWAS Ctlgrs10760502
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24762994] [Correlation Analysis of FPGS rs10760502G>A Polymorphism with Prognosis and MTX-related Toxicity in Pediatric B-cell Acute Lymphoblastic Leukemia]


[PMID 25765001] Association of FPGS genetic polymorphisms with primary retroperitoneal liposarcoma