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rs10486003

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10486003(C;T)
Make rs10486003(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position97600466
is asnp
is mentioned by
dbSNPrs10486003
ebirs10486003
HLIrs10486003
Exacrs10486003
Varsomers10486003
Maprs10486003
PheGenIrs10486003
hapmaprs10486003
1000 genomesrs10486003
hgdprs10486003
ensemblrs10486003
gopubmedrs10486003
geneviewrs10486003
scholarrs10486003
googlers10486003
pharmgkbrs10486003
gwascentralrs10486003
openSNPrs10486003
23andMers10486003
23andMe allrs10486003
SNP Nexus

SNPshotrs10486003
SNPdbers10486003
MSV3drs10486003
GWAS Ctlgrs10486003
GMAF0.1157
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22020760]
Trait
Title Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients.
Risk Allele
P-val 5E-7
Odds Ratio 3.1300 None