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rs10090117

From SNPedia

Orientationplus
Stabilizedplus
Make rs10090117(C;C)
Make rs10090117(C;T)
Make rs10090117(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position18523725
is asnp
is mentioned by
dbSNPrs10090117
ebirs10090117
HLIrs10090117
Exacrs10090117
Varsomers10090117
Maprs10090117
PheGenIrs10090117
hapmaprs10090117
1000 genomesrs10090117
hgdprs10090117
ensemblrs10090117
gopubmedrs10090117
geneviewrs10090117
scholarrs10090117
googlers10090117
pharmgkbrs10090117
gwascentralrs10090117
openSNPrs10090117
23andMers10090117
23andMe allrs10090117
SNP Nexus

SNPshotrs10090117
SNPdbers10090117
MSV3drs10090117
GWAS Ctlgrs10090117
GMAF0.1869
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 2.38 [1.64-3.44]