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rs12699683

From SNPedia

Orientationplus
Stabilizedplus
Make rs12699683(G;G)
Make rs12699683(G;T)
Make rs12699683(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position15093502
is asnp
is mentioned by
dbSNPrs12699683
ebirs12699683
HLIrs12699683
Exacrs12699683
Varsomers12699683
Maprs12699683
PheGenIrs12699683
hapmaprs12699683
1000 genomesrs12699683
hgdprs12699683
ensemblrs12699683
gopubmedrs12699683
geneviewrs12699683
scholarrs12699683
googlers12699683
pharmgkbrs12699683
gwascentralrs12699683
openSNPrs12699683
23andMers12699683
23andMe allrs12699683
SNP Nexus

SNPshotrs12699683
SNPdbers12699683
MSV3drs12699683
GWAS Ctlgrs12699683
GMAF0.1194
Max Magnitude
? (G;G) (G;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 7E-6
Odds Ratio 3.66 [2.08-6.45]