rs17348202

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0

Make rs17348202(C;C)

Make rs17348202(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

221207458

is a	snp
is	mentioned by
dbSNP	rs17348202
dbSNP (classic)	rs17348202
ClinGen	rs17348202
ebi	rs17348202
HLI	rs17348202
Exac	rs17348202
Gnomad	rs17348202
Varsome	rs17348202
LitVar	rs17348202
Map	rs17348202
PheGenI	rs17348202
Biobank	rs17348202
1000 genomes	rs17348202
hgdp	rs17348202
ensembl	rs17348202
geneview	rs17348202
scholar	rs17348202
google	rs17348202
pharmgkb	rs17348202
gwascentral	rs17348202
openSNP	rs17348202
23andMe	rs17348202
SNPshot	rs17348202
SNPdbe	rs17348202
MSV3d	rs17348202
GWAS Ctlg	rs17348202

GMAF

0.03306

Max Magnitude

0

?	(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]