Have questions? Visit https://www.reddit.com/r/SNPedia

rs499818

From SNPedia

Orientationplus
Stabilizedplus
Make rs499818(A;A)
Make rs499818(A;G)
Make rs499818(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position13332235
is asnp
is mentioned by
dbSNPrs499818
ebirs499818
HLIrs499818
Exacrs499818
Varsomers499818
Maprs499818
PheGenIrs499818
hapmaprs499818
1000 genomesrs499818
hgdprs499818
ensemblrs499818
gopubmedrs499818
geneviewrs499818
scholarrs499818
googlers499818
pharmgkbrs499818
gwascentralrs499818
openSNPrs499818
23andMers499818
23andMe allrs499818
SNP Nexus

SNPshotrs499818
SNPdbers499818
MSV3drs499818
GWAS Ctlgrs499818
GMAF0.1873
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs499818
PubMedID [PMID 17903304OA-icon.png]
Condition Major CVD
Gene Intergenic
Risk Allele
pValue 7.00E-006
OR NA
95% CI



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


[PMID 20823317OA-icon.png] is-rSNP: a novel technique for in silico regulatory SNP detection.


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


GET Evidence
rs499818
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary



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