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rs11781551

From SNPedia

Orientationplus
Stabilizedplus
Make rs11781551(A;A)
Make rs11781551(A;G)
Make rs11781551(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position122395852
is asnp
is mentioned by
dbSNPrs11781551
ebirs11781551
HLIrs11781551
Exacrs11781551
Varsomers11781551
Maprs11781551
PheGenIrs11781551
hapmaprs11781551
1000 genomesrs11781551
hgdprs11781551
ensemblrs11781551
gopubmedrs11781551
geneviewrs11781551
scholarrs11781551
googlers11781551
pharmgkbrs11781551
gwascentralrs11781551
openSNPrs11781551
23andMers11781551
23andMe allrs11781551
SNP Nexus

SNPshotrs11781551
SNPdbers11781551
MSV3drs11781551
GWAS Ctlgrs11781551
GMAF0.2971
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21909108OA-icon.png]
Trait
Title Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
Risk Allele A
P-val 2E-11
Odds Ratio 0.0078 [0.01-0.01] unit decrease


[PMID 26520901] Impact of carotid atherosclerosis loci on cardiovascular events