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rs1533317

From SNPedia

Orientationplus
Stabilizedplus
Make rs1533317(C;C)
Make rs1533317(C;T)
Make rs1533317(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position35409009
is asnp
is mentioned by
dbSNPrs1533317
ebirs1533317
HLIrs1533317
Exacrs1533317
Varsomers1533317
Maprs1533317
PheGenIrs1533317
hapmaprs1533317
1000 genomesrs1533317
hgdprs1533317
ensemblrs1533317
gopubmedrs1533317
geneviewrs1533317
scholarrs1533317
googlers1533317
pharmgkbrs1533317
gwascentralrs1533317
openSNPrs1533317
23andMers1533317
23andMe allrs1533317
SNP Nexus

SNPshotrs1533317
SNPdbers1533317
MSV3drs1533317
GWAS Ctlgrs1533317
GMAF0.438
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 A
P-val 0.000002
Odds Ratio 0.14 [0.08-0.20] unit increase


GET Evidence
rs1533317
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.34375
summary