Gene entry
AGPAT2
1-acylglycerol-3-phosphate O-acyltransferase 2
- Chromosome
- 9
- Cytoband
- 9q34.3
- Variants (rsID)
- 12
AGPAT2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q34.3). Its official name is “1-acylglycerol-3-phosphate O-acyltransferase 2”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs142145391Benignsingle nucleotide variantMonogenic diabetes
- rs138994150Conflicting interpretationssingle nucleotide variantCongenital generalized lipodystrophy type 1
- rs142993240Conflicting interpretationssingle nucleotide variantMonogenic diabetes|Congenital generalized lipodystrophy type 1
- rs116807569Pathogenicsingle nucleotide variantCongenital generalized lipodystrophy type 1
- rs114782902Uncertain significancesingle nucleotide variantMonogenic diabetes
- rs886063722Uncertain significancesingle nucleotide variantCongenital generalized lipodystrophy type 1
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.