rs2338
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2338(A;A) |
Make rs2338(A;G) |
Make rs2338(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 1573378 |
Gene | LOC107986555 |
is a | snp |
is | mentioned by |
dbSNP | rs2338 |
dbSNP (classic) | rs2338 |
ClinGen | rs2338 |
ebi | rs2338 |
HLI | rs2338 |
Exac | rs2338 |
Gnomad | rs2338 |
Varsome | rs2338 |
LitVar | rs2338 |
Map | rs2338 |
PheGenI | rs2338 |
Biobank | rs2338 |
1000 genomes | rs2338 |
hgdp | rs2338 |
ensembl | rs2338 |
geneview | rs2338 |
scholar | rs2338 |
rs2338 | |
pharmgkb | rs2338 |
gwascentral | rs2338 |
openSNP | rs2338 |
23andMe | rs2338 |
SNPshot | rs2338 |
SNPdbe | rs2338 |
MSV3d | rs2338 |
GWAS Ctlg | rs2338 |
GMAF | 0.3329 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22020760] |
Trait | |
Title | Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients. |
Risk Allele | |
P-val | 0.000005 |
Odds Ratio | 2.2700 None |