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rs11671653

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11671653(A;A)
Make rs11671653(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10727810
GeneDNM2
is asnp
is mentioned by
dbSNPrs11671653
ebirs11671653
HLIrs11671653
Exacrs11671653
Varsomers11671653
Maprs11671653
PheGenIrs11671653
hapmaprs11671653
1000 genomesrs11671653
hgdprs11671653
ensemblrs11671653
gopubmedrs11671653
geneviewrs11671653
scholarrs11671653
googlers11671653
pharmgkbrs11671653
gwascentralrs11671653
openSNPrs11671653
23andMers11671653
23andMe allrs11671653
SNP Nexus

SNPshotrs11671653
SNPdbers11671653
MSV3drs11671653
GWAS Ctlgrs11671653
GMAF0.08081
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21347282OA-icon.png]
Trait
Title Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
Risk Allele A
P-val 9E-7
Odds Ratio 0.1075 [0.07-0.15] SD increase