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rs17027130

From SNPedia

Orientationplus
Stabilizedplus
Make rs17027130(C;C)
Make rs17027130(C;T)
Make rs17027130(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position41046491
is asnp
is mentioned by
dbSNPrs17027130
dbSNP (classic)rs17027130
ClinGenrs17027130
ebirs17027130
HLIrs17027130
Exacrs17027130
Gnomadrs17027130
Varsomers17027130
LitVarrs17027130
Maprs17027130
PheGenIrs17027130
Biobankrs17027130
1000 genomesrs17027130
hgdprs17027130
ensemblrs17027130
geneviewrs17027130
scholarrs17027130
googlers17027130
pharmgkbrs17027130
gwascentralrs17027130
openSNPrs17027130
23andMers17027130
SNPshotrs17027130
SNPdbers17027130
MSV3drs17027130
GWAS Ctlgrs17027130
GMAF0.1331
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23648065OA-icon.png]
Trait Adverse response to chemotherapy (neutropenia/leucopenia) (camptothecin)
Title Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
Risk Allele C
P-val 3E-6
Odds Ratio 2.87 [1.844-4.452]