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rs11066015

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs11066015(A;A)
Make rs11066015(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position111730205
GeneACAD10
is asnp
is mentioned by
dbSNPrs11066015
ebirs11066015
HLIrs11066015
Exacrs11066015
Varsomers11066015
Maprs11066015
PheGenIrs11066015
hapmaprs11066015
1000 genomesrs11066015
hgdprs11066015
ensemblrs11066015
gopubmedrs11066015
geneviewrs11066015
scholarrs11066015
googlers11066015
pharmgkbrs11066015
gwascentralrs11066015
openSNPrs11066015
23andMers11066015
23andMe allrs11066015
SNP Nexus

SNPshotrs11066015
SNPdbers11066015
MSV3drs11066015
GWAS Ctlgrs11066015
GMAF0.05739
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21642993]
Trait
Title Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations.
Risk Allele A
P-val 7E-21
Odds Ratio 1.3800 [1.29-1.48]


[PMID 23364394] A genome-wide association study of a coronary artery disease risk variant