Gene entry
SLC6A19
solute carrier family 6 member 19
- Chromosome
- 5
- Cytoband
- 5p15.33
- Variants (rsID)
- 24
SLC6A19 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5p15.33). Its official name is “solute carrier family 6 member 19”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs121434346Conflicting interpretationssingle nucleotide variantNeutral 1 amino acid transport defect|Hyperglycinuria|Iminoglycinuria|Neutral 1 amino acid transport defect|Hyperglycinuria
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.