rs503662
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs503662(A;A) |
Make rs503662(A;G) |
Make rs503662(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 21191270 |
is a | snp |
is | mentioned by |
dbSNP | rs503662 |
dbSNP (classic) | rs503662 |
ClinGen | rs503662 |
ebi | rs503662 |
HLI | rs503662 |
Exac | rs503662 |
Gnomad | rs503662 |
Varsome | rs503662 |
LitVar | rs503662 |
Map | rs503662 |
PheGenI | rs503662 |
Biobank | rs503662 |
1000 genomes | rs503662 |
hgdp | rs503662 |
ensembl | rs503662 |
geneview | rs503662 |
scholar | rs503662 |
rs503662 | |
pharmgkb | rs503662 |
gwascentral | rs503662 |
openSNP | rs503662 |
23andMe | rs503662 |
SNPshot | rs503662 |
SNPdbe | rs503662 |
MSV3d | rs503662 |
GWAS Ctlg | rs503662 |
GMAF | 0.303 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23653095] Positive correlation between variants of lipid metabolism‑related genes and coronary heart disease
[PMID 21347282] Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.