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rs7027989

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1.26x increased myocardial infarction risk
(A;G) 1.26x increased myocardial infarction risk
(G;G) normal
ReferenceGRCh38 38.1/141
Chromosome9
Position21817755
GeneMTAP
is asnp
is mentioned by
dbSNPrs7027989
ebirs7027989
HLIrs7027989
Exacrs7027989
Varsomers7027989
Maprs7027989
PheGenIrs7027989
hapmaprs7027989
1000 genomesrs7027989
hgdprs7027989
ensemblrs7027989
gopubmedrs7027989
geneviewrs7027989
scholarrs7027989
googlers7027989
pharmgkbrs7027989
gwascentralrs7027989
openSNPrs7027989
23andMers7027989
23andMe allrs7027989
SNP Nexus

SNPshotrs7027989
SNPdbers7027989
MSV3drs7027989
GWAS Ctlgrs7027989
GMAF0.3352
Max Magnitude
? (A;A) (A;G) (G;G) 28
rs7027989 is a SNP in the methylthioadenosine phosphorylase MTAP gene.

A study of 432 Han Chinese patients with myocardial infarctions concluded that male subjects carrying a rs7027989(A) allele were at 1.26x increased risk (for MI).[PMID 19272367]


[PMID 20302706] [Association between methylthioadenosine phosphorylase gene single nucleotide polymorphisms and myocardial infarction in Chinese Han ethnicity.].