rs10090117

Orientation

plus

Stabilized

plus

Make rs10090117(C;C)

Make rs10090117(C;T)

Make rs10090117(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

18523725

is a	snp
is	mentioned by
dbSNP	rs10090117
dbSNP (classic)	rs10090117
ClinGen	rs10090117
ebi	rs10090117
HLI	rs10090117
Exac	rs10090117
Gnomad	rs10090117
Varsome	rs10090117
LitVar	rs10090117
Map	rs10090117
PheGenI	rs10090117
Biobank	rs10090117
1000 genomes	rs10090117
hgdp	rs10090117
ensembl	rs10090117
geneview	rs10090117
scholar	rs10090117
google	rs10090117
pharmgkb	rs10090117
gwascentral	rs10090117
openSNP	rs10090117
23andMe	rs10090117
SNPshot	rs10090117
SNPdbe	rs10090117
MSV3d	rs10090117
GWAS Ctlg	rs10090117

GMAF

0.1869

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	4E-6
Odds Ratio	2.38 [1.64-3.44]