Gene entry
BAAT
bile acid-CoA:amino acid N-acyltransferase
- Chromosome
- 9
- Cytoband
- 9q31.1
- Variants (rsID)
- 11
BAAT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q31.1). Its official name is “bile acid-CoA:amino acid N-acyltransferase”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs140793591Benignsingle nucleotide variantHypercholanemia, familial 1
- rs144591246Benignsingle nucleotide variantHypercholanemia, familial 1
- rs1572983Benignsingle nucleotide variantHypercholanemia, familial 1|Bile acid conjugation defect 1
- rs61755096Benignsingle nucleotide variantHypercholanemia, familial 1
- rs7043029Benignsingle nucleotide variantHypercholanemia, familial 1
- rs28937579Pathogenicsingle nucleotide variantBile acid conjugation defect 1
- rs138613717Uncertain significancesingle nucleotide variant
- rs190174945Uncertain significancesingle nucleotide variant
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.