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rs11479

From SNPedia

Orientationminus
Stabilizedminus
Make rs11479(C;C)
Make rs11479(C;T)
Make rs11479(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position50525807
GeneSCO2, TYMP
is asnp
is mentioned by
dbSNPrs11479
ebirs11479
HLIrs11479
Exacrs11479
Varsomers11479
Maprs11479
PheGenIrs11479
hapmaprs11479
1000 genomesrs11479
hgdprs11479
ensemblrs11479
gopubmedrs11479
geneviewrs11479
scholarrs11479
googlers11479
pharmgkbrs11479
gwascentralrs11479
openSNPrs11479
23andMers11479
23andMe allrs11479
SNP Nexus

SNPshotrs11479
SNPdbers11479
MSV3drs11479
GWAS Ctlgrs11479
Max Magnitude

[PMID 25027354OA-icon.png] Thymidine phosphorylase gene variant, platelet counts and survival in gastrointestinal cancer patients treated by fluoropyrimidines

ClinVar
Risk rs11479(A,G,T;A,G,T)
Alt rs11479(A,G,T;A,G,T)
Reference rs11479(C;C)
Significance Other
Disease not specified
Variation info
Gene TYMP SCO2
CLNDBN not specified
Reversed 1
HGVS NC_000022.10:g.50964236G>A
CLNSRC ClinVar GeneDx University of Chicago
CLNACC RCV000118807.3,