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rs12552736

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs12552736(C;C)
Make rs12552736(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position25449124
is asnp
is mentioned by
dbSNPrs12552736
ebirs12552736
HLIrs12552736
Exacrs12552736
Varsomers12552736
Maprs12552736
PheGenIrs12552736
hapmaprs12552736
1000 genomesrs12552736
hgdprs12552736
ensemblrs12552736
gopubmedrs12552736
geneviewrs12552736
scholarrs12552736
googlers12552736
pharmgkbrs12552736
gwascentralrs12552736
openSNPrs12552736
23andMers12552736
23andMe allrs12552736
SNP Nexus

SNPshotrs12552736
SNPdbers12552736
MSV3drs12552736
GWAS Ctlgrs12552736
GMAF0.1019
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20031603OA-icon.png]
Trait RR interval (heart rate)
Title A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations: The EUROSPAN Project
Risk Allele G
P-val 0.000002
Odds Ratio 0.25 [0.15-0.35] unit increase


GET Evidence
rs12552736
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.161017
summary