Rs27388
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs27388 |
| hapmap | rs27388 |
| hgdp | rs27388 |
| ensembl | rs27388 |
| gopubmed | rs27388 |
| scholar | rs27388 |
| rs27388 | |
| pharmgkb | rs27388 |
| hgvbaseg2p | rs27388 |
| medrefsnp | rs27388 |
| 23andMe | rs27388 |
| SNP Nexus |
| Gene | MEGF10 |
| Chromosome | 5 |
| Orientation | plus |
| Position | 126711707 |
| Genotype | Effect |
|---|---|
| rs27388(A;A) | somewhat increased risk for schizophrenia |
| rs27388(A;G) | somewhat increased risk for schizophrenia |
| rs27388(G;G) | normal risk |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs27388(A;A) | somewhat increased risk for schizophrenia | |
| Rs27388(A;G) | somewhat increased risk for schizophrenia | |
| Rs27388(G;G) | 00 | normal risk |
In a case-control study involving 652 Irish patients, rs27388(A) allele carriers were at increased risk for schizophrenia. (Note that the (A) allele is quite common in many populations.)[PMID 18179784]
| ? | (A;A) (A;G) (G;G) |
|---|---|
|
| |
