Gene entry
SLC18A1
solute carrier family 18 member A1
- Chromosome
- 8
- Cytoband
- 8p21.3
- Variants (rsID)
- 21
SLC18A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8p21.3). Its official name is “solute carrier family 18 member A1”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs1390938Not classifiedmissense_variantAutism|Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome|Autism Spectrum Disorder|Major Affective Disorder 8|Major Affective Disorder 9|Bipolar Disorder|Alcohol Dependence|Mental Depression|Major Depressive Disorder|Depression|Alcohol Use Disorder|Anxiety
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.