Rs10134944
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs10134944 |
| hapmap | rs10134944 |
| hgdp | rs10134944 |
| ensembl | rs10134944 |
| gopubmed | rs10134944 |
| scholar | rs10134944 |
| rs10134944 | |
| pharmgkb | rs10134944 |
| hgvbaseg2p | rs10134944 |
| medrefsnp | rs10134944 |
| 23andMe | rs10134944 |
| SNP Nexus |
| Chromosome | 14 |
| Orientation | plus |
| Position | 57188948 |
| Genotype | Effect |
|---|---|
| rs10134944(T;T) | 1.3x risk |
| rs10134944(C;T) | 1.4x risk |
| rs10134944(C;C) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs10134944(C;C) | 00 | normal |
| Rs10134944(C;T) | 1.4x risk | |
| Rs10134944(T;T) | 1.3x risk |
The risk allele (oriented to the dbSNP entry) is (T); the odds ratio associated with heterozygotes is 1.45 (CI 1.24-1.68), and for homozygotes, 1.32 (CI 0.74-2.33). [PMID 17554300]
| ? | (C;C) (C;T) (T;T) |
|---|---|
|
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