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rs12733856

From SNPedia

Orientationplus
Stabilizedplus
Make rs12733856(A;A)
Make rs12733856(A;C)
Make rs12733856(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position221378197
is asnp
is mentioned by
dbSNPrs12733856
ebirs12733856
HLIrs12733856
Exacrs12733856
Varsomers12733856
Maprs12733856
PheGenIrs12733856
hapmaprs12733856
1000 genomesrs12733856
hgdprs12733856
ensemblrs12733856
gopubmedrs12733856
geneviewrs12733856
scholarrs12733856
googlers12733856
pharmgkbrs12733856
gwascentralrs12733856
openSNPrs12733856
23andMers12733856
23andMe allrs12733856
SNP Nexus

SNPshotrs12733856
SNPdbers12733856
MSV3drs12733856
GWAS Ctlgrs12733856
GMAF0.3903
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 0.000003
Odds Ratio 1.56 [0.97-2.51]