Variant (rsID / SNP)
rs794728636
rs794728636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEN1. Location: chromosome 11, position 64,577,524. Clinical significance in the table: Pathogenic.
Reference-table entries
MEN1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Insertion
- Chromosome / position
- 11:64577524
- Cytoband
- 11q13.1
- HGVS
- NM_001370259.2(MEN1):c.57_58insT (p.Val20fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.