Variant (rsID / SNP)
rs878855196
rs878855196 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEN1. Location: chromosome 11, position 64,575,384. Clinical significance in the table: Pathogenic.
Reference-table entries
MEN1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 11:64575384
- Cytoband
- 11q13.1
- HGVS
- NM_001370259.2(MEN1):c.633del (p.Asn212fs)
Associated conditions / phenotypes
Multiple endocrine neoplasia, type 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.