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rs7318731

From SNPedia

Orientationplus
Stabilizedplus
Make rs7318731(A;A)
Make rs7318731(A;C)
Make rs7318731(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position22135531
is asnp
is mentioned by
dbSNPrs7318731
ebirs7318731
HLIrs7318731
Exacrs7318731
Varsomers7318731
Maprs7318731
PheGenIrs7318731
hapmaprs7318731
1000 genomesrs7318731
hgdprs7318731
ensemblrs7318731
gopubmedrs7318731
geneviewrs7318731
scholarrs7318731
googlers7318731
pharmgkbrs7318731
gwascentralrs7318731
openSNPrs7318731
23andMers7318731
23andMe allrs7318731
SNP Nexus

SNPshotrs7318731
SNPdbers7318731
MSV3drs7318731
GWAS Ctlgrs7318731
GMAF0.3531
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 0.000001
Odds Ratio 0.14 [0.08-0.20] unit decrease


GET Evidence
rs7318731
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.65873
summary