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rs840616

From SNPedia

Orientationplus
Stabilizedplus
Make rs840616(C;C)
Make rs840616(C;T)
Make rs840616(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position187331742
is asnp
is mentioned by
dbSNPrs840616
ebirs840616
HLIrs840616
Exacrs840616
Varsomers840616
Maprs840616
PheGenIrs840616
hapmaprs840616
1000 genomesrs840616
hgdprs840616
ensemblrs840616
gopubmedrs840616
geneviewrs840616
scholarrs840616
googlers840616
pharmgkbrs840616
gwascentralrs840616
openSNPrs840616
23andMers840616
23andMe allrs840616
SNP Nexus

SNPshotrs840616
SNPdbers840616
MSV3drs840616
GWAS Ctlgrs840616
GMAF0.3843
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21378988]
Trait
Title A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
Risk Allele
P-val 7E-7
Odds Ratio None None