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rs11598702

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs11598702(C;C)
Make rs11598702(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position103138228
GeneNT5C2
is asnp
is mentioned by
dbSNPrs11598702
ebirs11598702
HLIrs11598702
Exacrs11598702
Varsomers11598702
Maprs11598702
PheGenIrs11598702
hapmaprs11598702
1000 genomesrs11598702
hgdprs11598702
ensemblrs11598702
gopubmedrs11598702
geneviewrs11598702
scholarrs11598702
googlers11598702
pharmgkbrs11598702
gwascentralrs11598702
openSNPrs11598702
23andMers11598702
23andMe allrs11598702
SNP Nexus

SNPshotrs11598702
SNPdbers11598702
MSV3drs11598702
GWAS Ctlgrs11598702
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs11598702(C;C)
Alt rs11598702(C;C)
Reference rs11598702(T;T)
Significance Drug-response
Disease gemcitabine response - Other
Variation info
Gene NT5C2
CLNDBN gemcitabine response - Other
Reversed 0
HGVS NC_000010.10:g.104897985T>C
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211359.1,