rs275456
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs275456(A;A) |
Make rs275456(A;C) |
Make rs275456(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 6813824 |
is a | snp |
is | mentioned by |
dbSNP | rs275456 |
dbSNP (classic) | rs275456 |
ClinGen | rs275456 |
ebi | rs275456 |
HLI | rs275456 |
Exac | rs275456 |
Gnomad | rs275456 |
Varsome | rs275456 |
LitVar | rs275456 |
Map | rs275456 |
PheGenI | rs275456 |
Biobank | rs275456 |
1000 genomes | rs275456 |
hgdp | rs275456 |
ensembl | rs275456 |
geneview | rs275456 |
scholar | rs275456 |
rs275456 | |
pharmgkb | rs275456 |
gwascentral | rs275456 |
openSNP | rs275456 |
23andMe | rs275456 |
SNPshot | rs275456 |
SNPdbe | rs275456 |
MSV3d | rs275456 |
GWAS Ctlg | rs275456 |
GMAF | 0.2199 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 3E-6 |
Odds Ratio | 2.26 [1.60-3.18] |