rs2269231
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2269231(A;A) |
Make rs2269231(A;T) |
Make rs2269231(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 46935752 |
Gene | CYP4A11 |
is a | snp |
is | mentioned by |
dbSNP | rs2269231 |
dbSNP (classic) | rs2269231 |
ClinGen | rs2269231 |
ebi | rs2269231 |
HLI | rs2269231 |
Exac | rs2269231 |
Gnomad | rs2269231 |
Varsome | rs2269231 |
LitVar | rs2269231 |
Map | rs2269231 |
PheGenI | rs2269231 |
Biobank | rs2269231 |
1000 genomes | rs2269231 |
hgdp | rs2269231 |
ensembl | rs2269231 |
geneview | rs2269231 |
scholar | rs2269231 |
rs2269231 | |
pharmgkb | rs2269231 |
gwascentral | rs2269231 |
openSNP | rs2269231 |
23andMe | rs2269231 |
SNPshot | rs2269231 |
SNPdbe | rs2269231 |
MSV3d | rs2269231 |
GWAS Ctlg | rs2269231 |
Max Magnitude | 0 |
[PMID 22804341] Haplotype-based case-control study of CYP4A11 gene and myocardial infarction [PMID 18300855] A haplotype of the CYP4A11 gene associated with essential hypertension in Japanese men.
[PMID 18484194] Haplotype-based case study of human CYP4A11 gene and cerebral infarction in Japanese subject.