Rs6684865
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs6684865 |
| hapmap | rs6684865 |
| hgdp | rs6684865 |
| ensembl | rs6684865 |
| gopubmed | rs6684865 |
| scholar | rs6684865 |
| rs6684865 | |
| pharmgkb | rs6684865 |
| hgvbaseg2p | rs6684865 |
| medrefsnp | rs6684865 |
| 23andMe | rs6684865 |
| SNP Nexus |
| Gene | rs6684865 |
| Chromosome | 1 |
| Orientation | plus |
| Position | 2536088 |
| Genotype | Effect |
|---|---|
| rs6684865(A;A) | 1.5x risk |
| rs6684865(A;G) | 1.2x risk |
| rs6684865(G;G) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs6684865(A;A) | 00 | 1.5x risk |
| Rs6684865(A;G) | 1.2x risk | |
| Rs6684865(G;G) | normal |
The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.27 (CI 1.02-1.56), and for homozygotes, 1.54 (CI 1.25-1.90). [PMID 17554300]
| ? | (A;A) (A;G) (G;G) |
|---|---|
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