Variant (rsID / SNP)
rs398124436
rs398124436 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEN1. Location: chromosome 11, position 64,571,953. Clinical significance in the table: Pathogenic.
Reference-table entries
MEN1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Duplication
- Chromosome / position
- 11:64571953
- Cytoband
- 11q13.1
- HGVS
- NM_001370259.2(MEN1):c.1685dup (p.Glu563fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.