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rs9961113

From SNPedia

Orientationplus
Stabilizedplus
Make rs9961113(C;C)
Make rs9961113(C;T)
Make rs9961113(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position77893443
is asnp
is mentioned by
dbSNPrs9961113
ebirs9961113
HLIrs9961113
Exacrs9961113
Varsomers9961113
Maprs9961113
PheGenIrs9961113
hapmaprs9961113
1000 genomesrs9961113
hgdprs9961113
ensemblrs9961113
gopubmedrs9961113
geneviewrs9961113
scholarrs9961113
googlers9961113
pharmgkbrs9961113
gwascentralrs9961113
openSNPrs9961113
23andMers9961113
23andMe allrs9961113
SNP Nexus

SNPshotrs9961113
SNPdbers9961113
MSV3drs9961113
GWAS Ctlgrs9961113
GMAF0.3774
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23648065]
Trait Adverse response to chemotherapy (neutropenia/leucopenia) (gemcitabine)
Title Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
Risk Allele C
P-val 1E-6
Odds Ratio 2.47 [1.706-3.584]