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rs2880058

From SNPedia

Orientationplus
Stabilizedplus
Make rs2880058(A;A)
Make rs2880058(A;G)
Make rs2880058(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position162044842
is asnp
is mentioned by
dbSNPrs2880058
ebirs2880058
HLIrs2880058
Exacrs2880058
Varsomers2880058
Maprs2880058
PheGenIrs2880058
hapmaprs2880058
1000 genomesrs2880058
hgdprs2880058
ensemblrs2880058
gopubmedrs2880058
geneviewrs2880058
scholarrs2880058
googlers2880058
pharmgkbrs2880058
gwascentralrs2880058
openSNPrs2880058
23andMers2880058
23andMe allrs2880058
SNP Nexus

SNPshotrs2880058
SNPdbers2880058
MSV3drs2880058
GWAS Ctlgrs2880058
GMAF0.45
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19019189OA-icon.png] QT interval rs3807375 rs2880058
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 2E-10
Odds Ratio 0.19 [0.13-0.25] unit increase


[PMID 20215044OA-icon.png] Relationship of Common Candidate Gene Variants to Electrocardiographic T-Wave Peak to T-Wave End Interval and T-Wave Morphology Parameters


GET Evidence
rs2880058
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507812
summary



[PMID 23092954OA-icon.png] SHAVE: shrinkage estimator measured for multiple visits increases power in GWAS of quantitative traits.