Have questions? Visit https://www.reddit.com/r/SNPedia

rs4743150

From SNPedia

Orientationplus
Stabilizedplus
Make rs4743150(C;C)
Make rs4743150(C;T)
Make rs4743150(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position97977842
is asnp
is mentioned by
dbSNPrs4743150
ebirs4743150
HLIrs4743150
Exacrs4743150
Varsomers4743150
Maprs4743150
PheGenIrs4743150
hapmaprs4743150
1000 genomesrs4743150
hgdprs4743150
ensemblrs4743150
gopubmedrs4743150
geneviewrs4743150
scholarrs4743150
googlers4743150
pharmgkbrs4743150
gwascentralrs4743150
openSNPrs4743150
23andMers4743150
23andMe allrs4743150
SNP Nexus

SNPshotrs4743150
SNPdbers4743150
MSV3drs4743150
GWAS Ctlgrs4743150
GMAF0.2319
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000005
Odds Ratio None None