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rs1447537

From SNPedia

Orientationplus
Stabilizedplus
Make rs1447537(A;A)
Make rs1447537(A;G)
Make rs1447537(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position84019462
is asnp
is mentioned by
dbSNPrs1447537
ebirs1447537
HLIrs1447537
Exacrs1447537
Varsomers1447537
Maprs1447537
PheGenIrs1447537
hapmaprs1447537
1000 genomesrs1447537
hgdprs1447537
ensemblrs1447537
gopubmedrs1447537
geneviewrs1447537
scholarrs1447537
googlers1447537
pharmgkbrs1447537
gwascentralrs1447537
openSNPrs1447537
23andMers1447537
23andMe allrs1447537
SNP Nexus

SNPshotrs1447537
SNPdbers1447537
MSV3drs1447537
GWAS Ctlgrs1447537
GMAF0.477
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000004
Odds Ratio 0.15 [0.09-0.21] unit decrease


GET Evidence
rs1447537
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.460317
summary