Variant (rsID / SNP)
rs587781238
rs587781238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBE3A. Location: chromosome 15, position 25,585,262. Clinical significance in the table: Pathogenic.
Reference-table entries
UBE3APathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Microsatellite
- Chromosome / position
- 15:25585262
- Cytoband
- 15q11.2
- HGVS
- NM_130839.5(UBE3A):c.2463GAT[1] (p.Met822del)
Associated conditions / phenotypes
Angelman syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.