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rs275456

From SNPedia

Orientationminus
Stabilizedminus
Make rs275456(A;A)
Make rs275456(A;C)
Make rs275456(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position6813824
is asnp
is mentioned by
dbSNPrs275456
ebirs275456
HLIrs275456
Exacrs275456
Varsomers275456
Maprs275456
PheGenIrs275456
hapmaprs275456
1000 genomesrs275456
hgdprs275456
ensemblrs275456
gopubmedrs275456
geneviewrs275456
scholarrs275456
googlers275456
pharmgkbrs275456
gwascentralrs275456
openSNPrs275456
23andMers275456
23andMe allrs275456
SNP Nexus

SNPshotrs275456
SNPdbers275456
MSV3drs275456
GWAS Ctlgrs275456
GMAF0.2199
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23776197]
Trait Paclitaxel-induced neuropathy
Title Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy.
Risk Allele A
P-val 3E-6
Odds Ratio 2.26 [1.60-3.18]