Have questions? Visit https://www.reddit.com/r/SNPedia

rs7965445

From SNPedia

Orientationplus
Stabilizedplus
Make rs7965445(A;A)
Make rs7965445(A;G)
Make rs7965445(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position131378358
is asnp
is mentioned by
dbSNPrs7965445
ebirs7965445
HLIrs7965445
Exacrs7965445
Varsomers7965445
Maprs7965445
PheGenIrs7965445
hapmaprs7965445
1000 genomesrs7965445
hgdprs7965445
ensemblrs7965445
gopubmedrs7965445
geneviewrs7965445
scholarrs7965445
googlers7965445
pharmgkbrs7965445
gwascentralrs7965445
openSNPrs7965445
23andMers7965445
23andMe allrs7965445
SNP Nexus

SNPshotrs7965445
SNPdbers7965445
MSV3drs7965445
GWAS Ctlgrs7965445
GMAF0.1534
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000002
Odds Ratio 1.30 [0.99-1.72]