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rs11066001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs11066001(C;C)
Make rs11066001(C;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position111681367
GeneBRAP
is asnp
is mentioned by
dbSNPrs11066001
ebirs11066001
HLIrs11066001
Exacrs11066001
Varsomers11066001
Maprs11066001
PheGenIrs11066001
hapmaprs11066001
1000 genomesrs11066001
hgdprs11066001
ensemblrs11066001
gopubmedrs11066001
geneviewrs11066001
scholarrs11066001
googlers11066001
pharmgkbrs11066001
gwascentralrs11066001
openSNPrs11066001
23andMers11066001
23andMe allrs11066001
SNP Nexus

SNPshotrs11066001
SNPdbers11066001
MSV3drs11066001
GWAS Ctlgrs11066001
GMAF0.05647
Max Magnitude0

[PMID 19713974] Validation of eight genetic risk factors in East Asian populations replicated the association of BRAP with coronary artery disease


[PMID 21301165] Polymorphism of 270 A>G in BRAP is Associated with Lower Ankle-Brachial Index in a Taiwanese Population


[PMID 22085839] Synergistic Effect between BRAP Polymorphism and Diabetes on the Extent of Coronary Atherosclerosis in the Chinese Population


[PMID 22122968] Additive Effect of ANRIL and BRAP Polymorphisms on Ankle-Brachial Index in a Taiwanese Population

[PMID 21670849OA-icon.png] BRAP Activates Inflammatory Cascades and Increases the Risk for Carotid Atherosclerosis.


[PMID 23356535OA-icon.png] Lack of association between a functional variant of the BRCA-1 related associated protein (BRAP) gene and ischemic stroke


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