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rs4528684

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4528684(C;T)
Make rs4528684(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position14240762
is asnp
is mentioned by
dbSNPrs4528684
ebirs4528684
HLIrs4528684
Exacrs4528684
Varsomers4528684
Maprs4528684
PheGenIrs4528684
hapmaprs4528684
1000 genomesrs4528684
hgdprs4528684
ensemblrs4528684
gopubmedrs4528684
geneviewrs4528684
scholarrs4528684
googlers4528684
pharmgkbrs4528684
gwascentralrs4528684
openSNPrs4528684
23andMers4528684
23andMe allrs4528684
SNP Nexus

SNPshotrs4528684
SNPdbers4528684
MSV3drs4528684
GWAS Ctlgrs4528684
GMAF0.101
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20400778OA-icon.png]
Trait Mortality among heart failure patients
Title Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium
Risk Allele T
P-val 0.000001
Odds Ratio 1.42 [0.99-2.03]