rs10512385
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10512385(A;A) |
Make rs10512385(A;G) |
Make rs10512385(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 108693295 |
is a | snp |
is | mentioned by |
dbSNP | rs10512385 |
dbSNP (classic) | rs10512385 |
ClinGen | rs10512385 |
ebi | rs10512385 |
HLI | rs10512385 |
Exac | rs10512385 |
Gnomad | rs10512385 |
Varsome | rs10512385 |
LitVar | rs10512385 |
Map | rs10512385 |
PheGenI | rs10512385 |
Biobank | rs10512385 |
1000 genomes | rs10512385 |
hgdp | rs10512385 |
ensembl | rs10512385 |
geneview | rs10512385 |
scholar | rs10512385 |
rs10512385 | |
pharmgkb | rs10512385 |
gwascentral | rs10512385 |
openSNP | rs10512385 |
23andMe | rs10512385 |
SNPshot | rs10512385 |
SNPdbe | rs10512385 |
MSV3d | rs10512385 |
GWAS Ctlg | rs10512385 |
GMAF | 0.1208 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 6E-6 |
Odds Ratio | 2.58 [1.71-3.89] |