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rs12638540

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs12638540(A;G)
Make rs12638540(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position32447042
GeneCMTM7
is asnp
is mentioned by
dbSNPrs12638540
ebirs12638540
HLIrs12638540
Exacrs12638540
Varsomers12638540
Maprs12638540
PheGenIrs12638540
hapmaprs12638540
1000 genomesrs12638540
hgdprs12638540
ensemblrs12638540
gopubmedrs12638540
geneviewrs12638540
scholarrs12638540
googlers12638540
pharmgkbrs12638540
gwascentralrs12638540
openSNPrs12638540
23andMers12638540
23andMe allrs12638540
SNP Nexus

SNPshotrs12638540
SNPdbers12638540
MSV3drs12638540
GWAS Ctlgrs12638540
GMAF0.04545
Max Magnitude0
? (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 G
P-val 3E-7
Odds Ratio 1.53 [1.01-2.31]