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rs2478333

From SNPedia

Orientationplus
Stabilizedplus
Make rs2478333(A;A)
Make rs2478333(A;C)
Make rs2478333(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position47588423
is asnp
is mentioned by
dbSNPrs2478333
ebirs2478333
HLIrs2478333
Exacrs2478333
Varsomers2478333
Maprs2478333
PheGenIrs2478333
hapmaprs2478333
1000 genomesrs2478333
hgdprs2478333
ensemblrs2478333
gopubmedrs2478333
geneviewrs2478333
scholarrs2478333
googlers2478333
pharmgkbrs2478333
gwascentralrs2478333
openSNPrs2478333
23andMers2478333
23andMe allrs2478333
SNP Nexus

SNPshotrs2478333
SNPdbers2478333
MSV3drs2478333
GWAS Ctlgrs2478333
GMAF0.1837
Max Magnitude
? (A;A) (A;C) (C;C) 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 4E-8
Odds Ratio 0.17 [0.11-0.23] unit increase


GET Evidence
rs2478333
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary