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rs10512385

From SNPedia

Orientationplus
Stabilizedplus
Make rs10512385(A;A)
Make rs10512385(A;G)
Make rs10512385(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position108693295
is asnp
is mentioned by
dbSNPrs10512385
ebirs10512385
HLIrs10512385
Exacrs10512385
Varsomers10512385
Maprs10512385
PheGenIrs10512385
hapmaprs10512385
1000 genomesrs10512385
hgdprs10512385
ensemblrs10512385
gopubmedrs10512385
geneviewrs10512385
scholarrs10512385
googlers10512385
pharmgkbrs10512385
gwascentralrs10512385
openSNPrs10512385
23andMers10512385
23andMe allrs10512385
SNP Nexus

SNPshotrs10512385
SNPdbers10512385
MSV3drs10512385
GWAS Ctlgrs10512385
GMAF0.1208
Max Magnitude
? (A;A) (A;G) (G;G) 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 6E-6
Odds Ratio 2.58 [1.71-3.89]