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rs12882718

From SNPedia

Orientationplus
Stabilizedplus
Make rs12882718(C;C)
Make rs12882718(C;T)
Make rs12882718(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position86435710
is asnp
is mentioned by
dbSNPrs12882718
ebirs12882718
HLIrs12882718
Exacrs12882718
Varsomers12882718
Maprs12882718
PheGenIrs12882718
hapmaprs12882718
1000 genomesrs12882718
hgdprs12882718
ensemblrs12882718
gopubmedrs12882718
geneviewrs12882718
scholarrs12882718
googlers12882718
pharmgkbrs12882718
gwascentralrs12882718
openSNPrs12882718
23andMers12882718
23andMe allrs12882718
SNP Nexus

SNPshotrs12882718
SNPdbers12882718
MSV3drs12882718
GWAS Ctlgrs12882718
GMAF0.3958
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23648065]
Trait Adverse response to chemotherapy (neutropenia/leucopenia) (all antimicrotubule drugs)
Title Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
Risk Allele T
P-val 6E-6
Odds Ratio 1.56 [1.283-1.884]