rs6941513
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6941513(A;A) |
Make rs6941513(A;G) |
Make rs6941513(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 163609768 |
is a | snp |
is | mentioned by |
dbSNP | rs6941513 |
dbSNP (classic) | rs6941513 |
ClinGen | rs6941513 |
ebi | rs6941513 |
HLI | rs6941513 |
Exac | rs6941513 |
Gnomad | rs6941513 |
Varsome | rs6941513 |
LitVar | rs6941513 |
Map | rs6941513 |
PheGenI | rs6941513 |
Biobank | rs6941513 |
1000 genomes | rs6941513 |
hgdp | rs6941513 |
ensembl | rs6941513 |
geneview | rs6941513 |
scholar | rs6941513 |
rs6941513 | |
pharmgkb | rs6941513 |
gwascentral | rs6941513 |
openSNP | rs6941513 |
23andMe | rs6941513 |
SNPshot | rs6941513 |
SNPdbe | rs6941513 |
MSV3d | rs6941513 |
GWAS Ctlg | rs6941513 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26950853] Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.