rs3181157
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3181157(C;C) |
Make rs3181157(C;T) |
Make rs3181157(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 6199357 |
Gene | CD9 |
is a | snp |
is | mentioned by |
dbSNP | rs3181157 |
dbSNP (classic) | rs3181157 |
ClinGen | rs3181157 |
ebi | rs3181157 |
HLI | rs3181157 |
Exac | rs3181157 |
Gnomad | rs3181157 |
Varsome | rs3181157 |
LitVar | rs3181157 |
Map | rs3181157 |
PheGenI | rs3181157 |
Biobank | rs3181157 |
1000 genomes | rs3181157 |
hgdp | rs3181157 |
ensembl | rs3181157 |
geneview | rs3181157 |
scholar | rs3181157 |
rs3181157 | |
pharmgkb | rs3181157 |
gwascentral | rs3181157 |
openSNP | rs3181157 |
23andMe | rs3181157 |
SNPshot | rs3181157 |
SNPdbe | rs3181157 |
MSV3d | rs3181157 |
GWAS Ctlg | rs3181157 |
GMAF | 0.1777 |
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 | A |
P-val | 4E-6 |
Odds Ratio | 3.22 [1.96-5.29] |