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rs11921014

From SNPedia

Orientationplus
Stabilizedplus
Make rs11921014(A;A)
Make rs11921014(A;C)
Make rs11921014(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position141657298
is asnp
is mentioned by
dbSNPrs11921014
dbSNP (old)rs11921014
ClinGenrs11921014
ebirs11921014
HLIrs11921014
Exacrs11921014
Varsomers11921014
Maprs11921014
PheGenIrs11921014
Biobankrs11921014
1000 genomesrs11921014
hgdprs11921014
ensemblrs11921014
gopubmedrs11921014
geneviewrs11921014
scholarrs11921014
googlers11921014
pharmgkbrs11921014
gwascentralrs11921014
openSNPrs11921014
23andMers11921014
23andMe allrs11921014
SNP Nexus

SNPshotrs11921014
SNPdbers11921014
MSV3drs11921014
GWAS Ctlgrs11921014
GMAF0.02388
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23870195OA-icon.png]
Trait Coronary artery calcification
Title Genetics of coronary artery calcification among African Americans, a meta-analysis.
Risk Allele A
P-val 8E-6
Odds Ratio 1.07 [0.6-1.54] unit increase