rs7027989
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 1.26x increased myocardial infarction risk | |
(A;G) | 1.26x increased myocardial infarction risk | |
(G;G) | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 21817755 |
Gene | MTAP |
is a | snp |
is | mentioned by |
dbSNP | rs7027989 |
dbSNP (classic) | rs7027989 |
ClinGen | rs7027989 |
ebi | rs7027989 |
HLI | rs7027989 |
Exac | rs7027989 |
Gnomad | rs7027989 |
Varsome | rs7027989 |
LitVar | rs7027989 |
Map | rs7027989 |
PheGenI | rs7027989 |
Biobank | rs7027989 |
1000 genomes | rs7027989 |
hgdp | rs7027989 |
ensembl | rs7027989 |
geneview | rs7027989 |
scholar | rs7027989 |
rs7027989 | |
pharmgkb | rs7027989 |
gwascentral | rs7027989 |
openSNP | rs7027989 |
23andMe | rs7027989 |
SNPshot | rs7027989 |
SNPdbe | rs7027989 |
MSV3d | rs7027989 |
GWAS Ctlg | rs7027989 |
GMAF | 0.3352 |
Max Magnitude | 0 |
? | (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.].