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rs2549513

From SNPedia

Orientationplus
Stabilizedplus
Make rs2549513(A;A)
Make rs2549513(A;C)
Make rs2549513(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position79516830
is asnp
is mentioned by
dbSNPrs2549513
ebirs2549513
HLIrs2549513
Exacrs2549513
Varsomers2549513
Maprs2549513
PheGenIrs2549513
hapmaprs2549513
1000 genomesrs2549513
hgdprs2549513
ensemblrs2549513
gopubmedrs2549513
geneviewrs2549513
scholarrs2549513
googlers2549513
pharmgkbrs2549513
gwascentralrs2549513
openSNPrs2549513
23andMers2549513
23andMe allrs2549513
SNP Nexus

SNPshotrs2549513
SNPdbers2549513
MSV3drs2549513
GWAS Ctlgrs2549513
GMAF0.1529
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 22856164] [Evaluation of association between 9 genetic polymorphism and myocardial infarction in the Siberian population]


[PMID 17903304OA-icon.png] Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.


[PMID 20017983OA-icon.png] Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.


[PMID 22042884OA-icon.png] Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.


[PMID 24087953] [Genetic predictors of myocardial infarction in subjects of young age]