i5900852
From SNPedia
| 23andMe data | I5900852 |
| 23andMe search | I5900852 |
| opensnp | I5900852 |
| Gene (via rs) | MECP2 |
| iGeno | Mag | Summary |
|---|---|---|
| (D;D) | 0 | common/normal |
| alias | rs267608617 |
| Rs_StabilizedOrientation | minus |
| RsGeno | Mag | Summary |
|---|---|---|
| (-;TCTGCAAAGAGGAGAAGATGCCCAGA) | 6 | Rett syndrome (if accurately called) |
| (TCTGCAAAGAGGAGAAGATGCCCAGA;TCTGCAAAGAGGAGAAGATGCCCAGA) | 0 | common in clinvar |
However, note that the normal genotype as called by 23andMe is (D;D), even though this is actually the pathogenic (rare) mutation is a deletion, c.1235_1260del26 (p.Val412Glyfs).
