Promethease 0.1.82
Rs3212236
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs3212236 |
| hapmap | rs3212236 |
| hgdp | rs3212236 |
| ensembl | rs3212236 |
| gopubmed | rs3212236 |
| scholar | rs3212236 |
| rs3212236 | |
| pharmgkb | rs3212236 |
| hgvbaseg2p | rs3212236 |
| medrefsnp | rs3212236 |
| 23andMe | rs3212236 |
| SNP Nexus |
| Gene | TTRAP |
| Chromosome | 6 |
| Orientation | minus |
| Position | 24756434 |
| Genotype | Effect |
|---|---|
| rs3212236(A;A) | higher risk for dyslexia |
| rs3212236(A;G) | normal risk |
| rs3212236(G;G) | normal risk |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs3212236(A;A) | higher risk for dyslexia | |
| Rs3212236(A;G) | normal risk | |
| Rs3212236(C;T) | 00 | |
| Rs3212236(G;G) | normal risk |
The more common allele of rs3212236 has been linked to increased risk for developmental dyslexia in a study of ~300 British families. While odds ratios were not reported, the significance was reported as p=0.02.[PMID 17033633]
