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rs1895302

From SNPedia

Orientationplus
Stabilizedplus
Make rs1895302(C;C)
Make rs1895302(C;T)
Make rs1895302(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position170115596
is asnp
is mentioned by
dbSNPrs1895302
ebirs1895302
HLIrs1895302
Exacrs1895302
Varsomers1895302
Maprs1895302
PheGenIrs1895302
hapmaprs1895302
1000 genomesrs1895302
hgdprs1895302
ensemblrs1895302
gopubmedrs1895302
geneviewrs1895302
scholarrs1895302
googlers1895302
pharmgkbrs1895302
gwascentralrs1895302
openSNPrs1895302
23andMers1895302
23andMe allrs1895302
SNP Nexus

SNPshotrs1895302
SNPdbers1895302
MSV3drs1895302
GWAS Ctlgrs1895302
GMAF0.4633
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23648065]
Trait Adverse response to chemotherapy (neutropenia/leucopenia) (all platinum-based drugs)
Title Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
Risk Allele C
P-val 7E-6
Odds Ratio 1.34 [1.132-1.587]