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rs10519210

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs10519210(G;G)
Make rs10519210(G;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position63445726
is asnp
is mentioned by
dbSNPrs10519210
ebirs10519210
HLIrs10519210
Exacrs10519210
Varsomers10519210
Maprs10519210
PheGenIrs10519210
hapmaprs10519210
1000 genomesrs10519210
hgdprs10519210
ensemblrs10519210
gopubmedrs10519210
geneviewrs10519210
scholarrs10519210
googlers10519210
pharmgkbrs10519210
gwascentralrs10519210
openSNPrs10519210
23andMers10519210
23andMe allrs10519210
SNP Nexus

SNPshotrs10519210
SNPdbers10519210
MSV3drs10519210
GWAS Ctlgrs10519210
GMAF0.06152
Max Magnitude0
? (G;G) (G;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 1E-8
Odds Ratio 1.53 [1.05-2.24]