Gene entry
AMN
amnion associated transmembrane protein
- Chromosome
- 14
- Cytoband
- 14q32.32
- Variants (rsID)
- 2
AMN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q32.32). Its official name is “amnion associated transmembrane protein”. The reference table lists 2 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs119478058Likely pathogenicsingle nucleotide variantImerslund-Grasbeck syndrome type 2|Imerslund-Grasbeck syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.