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rs1165472

From SNPedia

Orientationminus
Stabilizedplus
Make rs1165472(C;C)
Make rs1165472(C;T)
Make rs1165472(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position55642931
is asnp
is mentioned by
dbSNPrs1165472
ebirs1165472
HLIrs1165472
Exacrs1165472
Varsomers1165472
Maprs1165472
PheGenIrs1165472
hapmaprs1165472
1000 genomesrs1165472
hgdprs1165472
ensemblrs1165472
gopubmedrs1165472
geneviewrs1165472
scholarrs1165472
googlers1165472
pharmgkbrs1165472
gwascentralrs1165472
openSNPrs1165472
23andMers1165472
23andMe allrs1165472
SNP Nexus

SNPshotrs1165472
SNPdbers1165472
MSV3drs1165472
GWAS Ctlgrs1165472
GMAF0.2153
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 G
P-val 4E-6
Odds Ratio 2.36 [1.64-3.40]