rs529038
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | ||
(C;T) | 0 |
Make rs529038(A;G) |
Make rs529038(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 117301070 |
Gene | ROS1 |
is a | snp |
is | mentioned by |
dbSNP | rs529038 |
dbSNP (classic) | rs529038 |
ClinGen | rs529038 |
ebi | rs529038 |
HLI | rs529038 |
Exac | rs529038 |
Gnomad | rs529038 |
Varsome | rs529038 |
LitVar | rs529038 |
Map | rs529038 |
PheGenI | rs529038 |
Biobank | rs529038 |
1000 genomes | rs529038 |
hgdp | rs529038 |
ensembl | rs529038 |
geneview | rs529038 |
scholar | rs529038 |
rs529038 | |
pharmgkb | rs529038 |
gwascentral | rs529038 |
openSNP | rs529038 |
23andMe | rs529038 |
SNPshot | rs529038 |
SNPdbe | rs529038 |
MSV3d | rs529038 |
GWAS Ctlg | rs529038 |
GMAF | 0.1575 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19863298] rs529038, also known as Asp2213Asn, is not associated with coronary artery disease in a Greek case-control study of ~300 patients.
[PMID 16175505] Identification of four gene variants associated with myocardial infarction.
[PMID 18506375] Association of genetic variants with atherothrombotic cerebral infarction in Japanese individuals with metabolic syndrome.
[PMID 18599554] Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia.