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rs7728043

From SNPedia

Orientationplus
Stabilizedplus
Make rs7728043(C;C)
Make rs7728043(C;T)
Make rs7728043(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position5897581
is asnp
is mentioned by
dbSNPrs7728043
ebirs7728043
HLIrs7728043
Exacrs7728043
Varsomers7728043
Maprs7728043
PheGenIrs7728043
hapmaprs7728043
1000 genomesrs7728043
hgdprs7728043
ensemblrs7728043
gopubmedrs7728043
geneviewrs7728043
scholarrs7728043
googlers7728043
pharmgkbrs7728043
gwascentralrs7728043
openSNPrs7728043
23andMers7728043
23andMe allrs7728043
SNP Nexus

SNPshotrs7728043
SNPdbers7728043
MSV3drs7728043
GWAS Ctlgrs7728043
GMAF0.4591
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20031603OA-icon.png]
Trait QT interval
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 0.000001
Odds Ratio 0.14 [0.08-0.20] unit decrease


GET Evidence
rs7728043
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.53125
summary