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rs2338

From SNPedia

Orientationplus
Stabilizedplus
Make rs2338(A;A)
Make rs2338(A;G)
Make rs2338(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position1573378
is asnp
is mentioned by
dbSNPrs2338
ebirs2338
HLIrs2338
Exacrs2338
Varsomers2338
Maprs2338
PheGenIrs2338
hapmaprs2338
1000 genomesrs2338
hgdprs2338
ensemblrs2338
gopubmedrs2338
geneviewrs2338
scholarrs2338
googlers2338
pharmgkbrs2338
gwascentralrs2338
openSNPrs2338
23andMers2338
23andMe allrs2338
SNP Nexus

SNPshotrs2338
SNPdbers2338
MSV3drs2338
GWAS Ctlgrs2338
GMAF0.3329
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000005
Odds Ratio 2.2700 None