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rs2679073

From SNPedia

Orientationminus
Stabilizedminus
Make rs2679073(C;C)
Make rs2679073(C;T)
Make rs2679073(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position87434245
GeneLOC102724465
is asnp
is mentioned by
dbSNPrs2679073
ebirs2679073
HLIrs2679073
Exacrs2679073
Varsomers2679073
Maprs2679073
PheGenIrs2679073
hapmaprs2679073
1000 genomesrs2679073
hgdprs2679073
ensemblrs2679073
gopubmedrs2679073
geneviewrs2679073
scholarrs2679073
googlers2679073
pharmgkbrs2679073
gwascentralrs2679073
openSNPrs2679073
23andMers2679073
23andMe allrs2679073
SNP Nexus

SNPshotrs2679073
SNPdbers2679073
MSV3drs2679073
GWAS Ctlgrs2679073
GMAF0.02755
Max Magnitude
? (C;C) (C;T) (T;T) 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 4E-6
Odds Ratio 1.50 [0.85-2.15] unit decrease