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rs563519

From SNPedia

Orientationplus
Stabilizedplus
Make rs563519(C;C)
Make rs563519(C;T)
Make rs563519(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position126158822
is asnp
is mentioned by
dbSNPrs563519
ebirs563519
HLIrs563519
Exacrs563519
Varsomers563519
Maprs563519
PheGenIrs563519
hapmaprs563519
1000 genomesrs563519
hgdprs563519
ensemblrs563519
gopubmedrs563519
geneviewrs563519
scholarrs563519
googlers563519
pharmgkbrs563519
gwascentralrs563519
openSNPrs563519
23andMers563519
23andMe allrs563519
SNP Nexus

SNPshotrs563519
SNPdbers563519
MSV3drs563519
GWAS Ctlgrs563519
GMAF0.4486
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20445134OA-icon.png]
Trait Heart failure
Title The Association of Genome-Wide Variation with the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis from the CHARGE Consortium
Risk Allele
P-val 0.000003
Odds Ratio 1.45 [0.97-2.17]