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rs3181157

From SNPedia

Orientationplus
Stabilizedplus
Make rs3181157(C;C)
Make rs3181157(C;T)
Make rs3181157(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position6199357
GeneCD9
is asnp
is mentioned by
dbSNPrs3181157
ebirs3181157
HLIrs3181157
Exacrs3181157
Varsomers3181157
Maprs3181157
PheGenIrs3181157
hapmaprs3181157
1000 genomesrs3181157
hgdprs3181157
ensemblrs3181157
gopubmedrs3181157
geneviewrs3181157
scholarrs3181157
googlers3181157
pharmgkbrs3181157
gwascentralrs3181157
openSNPrs3181157
23andMers3181157
23andMe allrs3181157
SNP Nexus

SNPshotrs3181157
SNPdbers3181157
MSV3drs3181157
GWAS Ctlgrs3181157
GMAF0.1777
Max Magnitude
? (C;C) (C;T) (T;T) 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 4E-6
Odds Ratio 3.22 [1.96-5.29]