Rs2639703
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs2639703 |
| hapmap | rs2639703 |
| hgdp | rs2639703 |
| ensembl | rs2639703 |
| gopubmed | rs2639703 |
| scholar | rs2639703 |
| rs2639703 | |
| pharmgkb | rs2639703 |
| hgvbaseg2p | rs2639703 |
| medrefsnp | rs2639703 |
| 23andMe | rs2639703 |
| SNP Nexus |
| Gene | ENAH |
| Chromosome | 1 |
| Orientation | plus |
| Position | 223879533 |
| Genotype | Effect |
|---|---|
| rs2639703(C;C) | 1.6x risk |
| rs2639703(C;T) | 1.1x risk |
| rs2639703(T;T) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs2639703(A;A) | 00 | |
| Rs2639703(C;C) | 1.6x risk | |
| Rs2639703(C;T) | 1.1x risk | |
| Rs2639703(T;T) | 00 | normal |
The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with heterozygotes is 1.15 (CI 1.02-1.31), and for homozygotes, 1.61 (CI 1.31-1.99). [PMID 17554300]
| ? | (C;C) (C;T) (T;T) |
|---|---|
|
| |
