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rs11047543

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs11047543(A;A)
Make rs11047543(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position24635405
is asnp
is mentioned by
dbSNPrs11047543
ebirs11047543
HLIrs11047543
Exacrs11047543
Varsomers11047543
Maprs11047543
PheGenIrs11047543
hapmaprs11047543
1000 genomesrs11047543
hgdprs11047543
ensemblrs11047543
gopubmedrs11047543
geneviewrs11047543
scholarrs11047543
googlers11047543
pharmgkbrs11047543
gwascentralrs11047543
openSNPrs11047543
23andMers11047543
23andMe allrs11047543
SNP Nexus

SNPshotrs11047543
SNPdbers11047543
MSV3drs11047543
GWAS Ctlgrs11047543
GMAF0.118
Max Magnitude0
? (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 A
P-val 3E-13
Odds Ratio 2.09 [1.53-2.65] ms decrease


[PMID 22336519] Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years

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


[PMID 24922963] 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease