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

rs4944092

From SNPedia

Orientationplus
Stabilizedplus
Make rs4944092(A;A)
Make rs4944092(A;G)
Make rs4944092(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position76198575
GeneWNT11
is asnp
is mentioned by
dbSNPrs4944092
ebirs4944092
HLIrs4944092
Exacrs4944092
Varsomers4944092
Maprs4944092
PheGenIrs4944092
hapmaprs4944092
1000 genomesrs4944092
hgdprs4944092
ensemblrs4944092
gopubmedrs4944092
geneviewrs4944092
scholarrs4944092
googlers4944092
pharmgkbrs4944092
gwascentralrs4944092
openSNPrs4944092
23andMers4944092
23andMe allrs4944092
SNP Nexus

SNPshotrs4944092
SNPdbers4944092
MSV3drs4944092
GWAS Ctlgrs4944092
GMAF0.3209
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20062060OA-icon.png]
Trait PR interval
Title Genome-wide association study of PR interval
Risk Allele G
P-val 3E-8
Odds Ratio 1.19 [0.77-1.61] ms decrease


[PMID 21347284OA-icon.png] Genome-wide association studies of the PR interval in African Americans.