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rs6961860

From SNPedia

Orientationplus
Stabilizedplus
Make rs6961860(C;C)
Make rs6961860(C;T)
Make rs6961860(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position17045697
is asnp
is mentioned by
dbSNPrs6961860
ebirs6961860
HLIrs6961860
Exacrs6961860
Varsomers6961860
Maprs6961860
PheGenIrs6961860
hapmaprs6961860
1000 genomesrs6961860
hgdprs6961860
ensemblrs6961860
gopubmedrs6961860
geneviewrs6961860
scholarrs6961860
googlers6961860
pharmgkbrs6961860
gwascentralrs6961860
openSNPrs6961860
23andMers6961860
23andMe allrs6961860
SNP Nexus

SNPshotrs6961860
SNPdbers6961860
MSV3drs6961860
GWAS Ctlgrs6961860
GMAF0.4164
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 G
P-val 5E-6
Odds Ratio 1.28 [1.078-1.527]