Have questions? Visit https://www.reddit.com/r/SNPedia

rs17348202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs17348202(C;C)
Make rs17348202(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position221207458
is asnp
is mentioned by
dbSNPrs17348202
ebirs17348202
HLIrs17348202
Exacrs17348202
Varsomers17348202
Maprs17348202
PheGenIrs17348202
hapmaprs17348202
1000 genomesrs17348202
hgdprs17348202
ensemblrs17348202
gopubmedrs17348202
geneviewrs17348202
scholarrs17348202
googlers17348202
pharmgkbrs17348202
gwascentralrs17348202
openSNPrs17348202
23andMers17348202
23andMe allrs17348202
SNP Nexus

SNPshotrs17348202
SNPdbers17348202
MSV3drs17348202
GWAS Ctlgrs17348202
GMAF0.03306
Max Magnitude0
? (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 1E-6
Odds Ratio 4.85 [2.57-9.13]