Have questions? Visit https://www.reddit.com/r/SNPedia

rs830884

From SNPedia

Orientationplus
Stabilizedplus
Make rs830884(C;C)
Make rs830884(C;T)
Make rs830884(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position52724562
is asnp
is mentioned by
dbSNPrs830884
ebirs830884
HLIrs830884
Exacrs830884
Varsomers830884
Maprs830884
PheGenIrs830884
hapmaprs830884
1000 genomesrs830884
hgdprs830884
ensemblrs830884
gopubmedrs830884
geneviewrs830884
scholarrs830884
googlers830884
pharmgkbrs830884
gwascentralrs830884
openSNPrs830884
23andMers830884
23andMe allrs830884
SNP Nexus

SNPshotrs830884
SNPdbers830884
MSV3drs830884
GWAS Ctlgrs830884
GMAF0.1157
Max Magnitude
? (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 0.000002
Odds Ratio 3.1300 None