rs1165472

Orientation

minus

Stabilized

minus

Make rs1165472(C;C)

Make rs1165472(C;T)

Make rs1165472(T;T)

Reference

GRCh38 38.1/142

Chromosome

1

Position

55642931

is a	snp
is	mentioned by
dbSNP	rs1165472
dbSNP (classic)	rs1165472
ClinGen	rs1165472
ebi	rs1165472
HLI	rs1165472
Exac	rs1165472
Gnomad	rs1165472
Varsome	rs1165472
LitVar	rs1165472
Map	rs1165472
PheGenI	rs1165472
Biobank	rs1165472
1000 genomes	rs1165472
hgdp	rs1165472
ensembl	rs1165472
geneview	rs1165472
scholar	rs1165472
google	rs1165472
pharmgkb	rs1165472
gwascentral	rs1165472
openSNP	rs1165472
23andMe	rs1165472
SNPshot	rs1165472
SNPdbe	rs1165472
MSV3d	rs1165472
GWAS Ctlg	rs1165472

GMAF

0.2153

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	2.36 [1.64-3.40]