rs4411227
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4411227(C;C) |
Make rs4411227(C;G) |
Make rs4411227(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 93071756 |
Gene | CYP26A1 |
is a | snp |
is | mentioned by |
dbSNP | rs4411227 |
dbSNP (classic) | rs4411227 |
ClinGen | rs4411227 |
ebi | rs4411227 |
HLI | rs4411227 |
Exac | rs4411227 |
Gnomad | rs4411227 |
Varsome | rs4411227 |
LitVar | rs4411227 |
Map | rs4411227 |
PheGenI | rs4411227 |
Biobank | rs4411227 |
1000 genomes | rs4411227 |
hgdp | rs4411227 |
ensembl | rs4411227 |
geneview | rs4411227 |
scholar | rs4411227 |
rs4411227 | |
pharmgkb | rs4411227 |
gwascentral | rs4411227 |
openSNP | rs4411227 |
23andMe | rs4411227 |
SNPshot | rs4411227 |
SNPdbe | rs4411227 |
MSV3d | rs4411227 |
GWAS Ctlg | rs4411227 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 25839051] Association Study between Novel CYP26 Polymorphisms and the Risk of Betel Quid-Related Malignant Oral Disorders