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rs11650066

From SNPedia

Orientationplus
Stabilizedplus
Make rs11650066(A;A)
Make rs11650066(A;G)
Make rs11650066(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position33960430
GeneASIC2
is asnp
is mentioned by
dbSNPrs11650066
ebirs11650066
HLIrs11650066
Exacrs11650066
Varsomers11650066
Maprs11650066
PheGenIrs11650066
hapmaprs11650066
1000 genomesrs11650066
hgdprs11650066
ensemblrs11650066
gopubmedrs11650066
geneviewrs11650066
scholarrs11650066
googlers11650066
pharmgkbrs11650066
gwascentralrs11650066
openSNPrs11650066
23andMers11650066
23andMe allrs11650066
SNP Nexus

SNPshotrs11650066
SNPdbers11650066
MSV3drs11650066
GWAS Ctlgrs11650066
GMAF0.3017
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21378988]
Trait
Title A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
Risk Allele
P-val 0.000006
Odds Ratio None None