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rs17019682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17019682(A;T)
Make rs17019682(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position91911494
is asnp
is mentioned by
dbSNPrs17019682
ebirs17019682
HLIrs17019682
Exacrs17019682
Varsomers17019682
Maprs17019682
PheGenIrs17019682
hapmaprs17019682
1000 genomesrs17019682
hgdprs17019682
ensemblrs17019682
gopubmedrs17019682
geneviewrs17019682
scholarrs17019682
googlers17019682
pharmgkbrs17019682
gwascentralrs17019682
openSNPrs17019682
23andMers17019682
23andMe allrs17019682
SNP Nexus

SNPshotrs17019682
SNPdbers17019682
MSV3drs17019682
GWAS Ctlgrs17019682
GMAF0.06566
Max Magnitude0
? (A;A) (A;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 0.000002
Odds Ratio 1.47 [0.98-2.22]