rs12699683

Orientation

plus

Stabilized

plus

Make rs12699683(G;G)

Make rs12699683(G;T)

Make rs12699683(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

15093502

is a	snp
is	mentioned by
dbSNP	rs12699683
dbSNP (classic)	rs12699683
ClinGen	rs12699683
ebi	rs12699683
HLI	rs12699683
Exac	rs12699683
Gnomad	rs12699683
Varsome	rs12699683
LitVar	rs12699683
Map	rs12699683
PheGenI	rs12699683
Biobank	rs12699683
1000 genomes	rs12699683
hgdp	rs12699683
ensembl	rs12699683
geneview	rs12699683
scholar	rs12699683
google	rs12699683
pharmgkb	rs12699683
gwascentral	rs12699683
openSNP	rs12699683
23andMe	rs12699683
SNPshot	rs12699683
SNPdbe	rs12699683
MSV3d	rs12699683
GWAS Ctlg	rs12699683

GMAF

0.1194

Max Magnitude

0

?	(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]