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rs6725887

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs6725887(C;C)
Make rs6725887(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position202881162
GeneWDR12
is asnp
is mentioned by
dbSNPrs6725887
dbSNP (classic)rs6725887
ClinGenrs6725887
ebirs6725887
HLIrs6725887
Exacrs6725887
Gnomadrs6725887
Varsomers6725887
LitVarrs6725887
Maprs6725887
PheGenIrs6725887
Biobankrs6725887
1000 genomesrs6725887
hgdprs6725887
ensemblrs6725887
geneviewrs6725887
scholarrs6725887
googlers6725887
pharmgkbrs6725887
gwascentralrs6725887
openSNPrs6725887
23andMers6725887
SNPshotrs6725887
SNPdbers6725887
MSV3drs6725887
GWAS Ctlgrs6725887
GMAF0.073
Max Magnitude0
? (C;C) (C;T) (T;T) 28


23andMe blog coronary artery disease and heart attack

SNP Risk Version Effect

GWAS snp
PMID [PMID 19198609OA-icon.png]
Trait Myocardial infarction (early onset)
Title Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Risk Allele C
P-val 1E-8
Odds Ratio 1.17 [1.11-1.23]



GWAS snp
PMID [PMID 21378990OA-icon.png]
Trait
Title Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Risk Allele C
P-val 1E-9
Odds Ratio 1.1400 [1.09-1.19]


[PMID 19956433OA-icon.png] Genetics of coronary artery disease: focus on genome-wide association studies.


[PMID 20835900OA-icon.png] Genetics of diabetes complications.


[PMID 21304891OA-icon.png] A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.


Coronary Heart Disease

GWAS snp
PMID [PMID 24262325OA-icon.png]
Trait Coronary artery disease
Title Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele C
P-val 2E-8
Odds Ratio 1.14 [1.10-1.19]


[PMID 25804320] Association Between Coronary Artery Disease Genetic Variants and Subclinical Atherosclerosis: an Association Study and Meta-analysis


[PMID 26629484OA-icon.png] Analysis of rs6725887 in the WD Repeat Protein 12 in Association with Coronary Artery Disease in Iranian Patients.


[PMID 28710368OA-icon.png] Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.