Rs4655595
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs4655595 |
| hapmap | rs4655595 |
| hgdp | rs4655595 |
| ensembl | rs4655595 |
| gopubmed | rs4655595 |
| scholar | rs4655595 |
| rs4655595 | |
| pharmgkb | rs4655595 |
| hgvbaseg2p | rs4655595 |
| medrefsnp | rs4655595 |
| 23andMe | rs4655595 |
| SNP Nexus |
| Gene | PDE4B |
| Chromosome | 1 |
| Orientation | plus |
| Position | 66331346 |
| Genotype | Effect |
|---|---|
| rs4655595(A;A) | normal |
| rs4655595(A;G) | 1.4 risk |
| rs4655595(G;G) | 2.3 risk |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs4655595(A;A) | normal | |
| Rs4655595(A;G) | 1.4 risk | |
| Rs4655595(G;G) | 2.3 risk |
The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.37 (CI 1.17-1.59), and for homozygotes, 2.33 (CI 1.23-4.42). [PMID 17554300]
| ? | (A;A) (A;G) (G;G) |
|---|---|
|
| |
