Rs7753394
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs7753394 |
| hapmap | rs7753394 |
| hgdp | rs7753394 |
| ensembl | rs7753394 |
| gopubmed | rs7753394 |
| scholar | rs7753394 |
| rs7753394 | |
| pharmgkb | rs7753394 |
| hgvbaseg2p | rs7753394 |
| medrefsnp | rs7753394 |
| 23andMe | rs7753394 |
| SNP Nexus |
| Chromosome | 6 |
| Orientation | plus |
| Position | 138126940 |
| Genotype | Effect |
|---|---|
| rs7753394(C;C) | 1.5x risk |
| rs7753394(C;T) | 1.2x risk |
| rs7753394(T;T) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs7753394(C;C) | 1.5x risk | |
| Rs7753394(C;T) | 1.2x risk | |
| Rs7753394(T;T) | 00 | normal |
The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.21 (CI 1.04-1.40), and for homozygotes, 1.48 (CI 1.25-1.76). [PMID 17554300]
| ? | (C;C) (C;T) (T;T) |
|---|---|
|
| |
