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rs3782886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs3782886(A;G)
Make rs3782886(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position111672685
GeneBRAP
is asnp
is mentioned by
dbSNPrs3782886
ebirs3782886
HLIrs3782886
Exacrs3782886
Varsomers3782886
Maprs3782886
PheGenIrs3782886
hapmaprs3782886
1000 genomesrs3782886
hgdprs3782886
ensemblrs3782886
gopubmedrs3782886
geneviewrs3782886
scholarrs3782886
googlers3782886
pharmgkbrs3782886
gwascentralrs3782886
openSNPrs3782886
23andMers3782886
23andMe allrs3782886
SNP Nexus

SNPshotrs3782886
SNPdbers3782886
MSV3drs3782886
GWAS Ctlgrs3782886
GMAF0.05739
Max Magnitude0
? (A;A) (A;G) (G;G) 28

23andMe blog coronary artery disease and heart attack

SNP Risk Version Effect

GWAS snp
PMID [PMID 20139978]
Trait Hematological and biochemical traits
Title Genome-wide association study of hematological and biochemical traits in a Japanese population
Risk Allele G
P-val 5E-9
Odds Ratio 0.25 [NR] % variance

Coronary Heart Disease


[PMID 22965072] The single nucleotide polymorphisms in BRAP decrease the risk of metabolic syndrome in a Chinese young adult population.

GWAS snp
PMID [PMID 24916648]
Trait Myocardial infarction
Title A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
Risk Allele A
P-val 1E-14
Odds Ratio 1.46 [1.33-1.60]