Variant (rsID / SNP)
rs1064795635
rs1064795635 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEN1. Location: chromosome 11, position 64,575,123. Clinical significance in the table: Likely pathogenic.
Reference-table entries
MEN1Likely pathogenic
- Clinical significance (as recorded)
- Likely pathogenic
- Variant type
- Deletion
- Chromosome / position
- 11:64575123
- Cytoband
- 11q13.1
- HGVS
- NM_001370259.2(MEN1):c.684del (p.Met228fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.