rs267608617(TCTGCAAAGAGGAGAAGATGCCCAGA;TCTGCAAAGAGGAGAAGATGCCCAGA)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs267608617 |
| Gene | MECP2 |
| Chromosome | X |
| Position | 154,030,568 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;TCTGCAAAGAGGAGAAGATGCCCAGA) | 6 | Rett syndrome (if accurately called) |
| (TCTGCAAAGAGGAGAAGATGCCCAGA;TCTGCAAAGAGGAGAAGATGCCCAGA) | 0 | common in clinvar |
