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rs7325568

From SNPedia

Orientationplus
Stabilizedplus
Make rs7325568(C;C)
Make rs7325568(C;T)
Make rs7325568(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position40244147
is asnp
is mentioned by
dbSNPrs7325568
dbSNP (classic)rs7325568
ClinGenrs7325568
ebirs7325568
HLIrs7325568
Exacrs7325568
Gnomadrs7325568
Varsomers7325568
LitVarrs7325568
Maprs7325568
PheGenIrs7325568
Biobankrs7325568
1000 genomesrs7325568
hgdprs7325568
ensemblrs7325568
geneviewrs7325568
scholarrs7325568
googlers7325568
pharmgkbrs7325568
gwascentralrs7325568
openSNPrs7325568
23andMers7325568
SNPshotrs7325568
SNPdbers7325568
MSV3drs7325568
GWAS Ctlgrs7325568
GMAF0.3838
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22310351] Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration.