Rs17465637
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs17465637 |
| hapmap | rs17465637 |
| hgdp | rs17465637 |
| ensembl | rs17465637 |
| gopubmed | rs17465637 |
| scholar | rs17465637 |
| rs17465637 | |
| pharmgkb | rs17465637 |
| hgvbaseg2p | rs17465637 |
| medrefsnp | rs17465637 |
| 23andMe | rs17465637 |
| SNP Nexus |
| Gene | MIA3 |
| Chromosome | 1 |
| Orientation | plus |
| Position | 220890151 |
| Genotype | Effect |
|---|---|
| rs17465637(A;A)* | ? |
| rs17465637(A;C)* | ? |
| rs17465637(C;C)* | ? |
spittoon coronary artery disease and heart attack
SNP Risk Version Effect
- rs646776 T 1.19
- rs17465637 C 1.14
- rs1746048 C 1.17
- rs6725887 C 1.17
- rs11206510 T 1.15
- rs3184504 T 1.13
- rs2306374 C 1.15
- rs3782886 C 1.44
| ? | (A;A) (A;C) (C;C) |
|---|---|
|
| |
| GWAS snp | |
|---|---|
| PMID | [PMID 19198609] |
| Trait | Myocardial infarction (early onset) |
| Title | Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants |
| Risk Allele | C |
| P-val | 1E-9 |
| Odds Ratio | 1.14 [1.10-1.19] |
| PharmGKB | PA162565803 |
| Name | |
| Annotation | In a genome-wide association study this variant (rs17465637) in MIA3 was associated with with early-onset myocardial infarction in 2,967 cases and 3,075 controls. |
| Gene | MIA3 |
| Featue | |
| Evidence | PubMed ID:19198609 |
| Drugs | |
| Diseases | Myocardial Infarction |
| Curation Level | Curated |
