Gene entry
SLC1A3
solute carrier family 1 member 3
- Chromosome
- 5
- Cytoband
- 5p13.2
- Variants (rsID)
- 38
SLC1A3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5p13.2). Its official name is “solute carrier family 1 member 3”. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs115702388Benignsingle nucleotide variantEpisodic ataxia type 6|Spastic ataxia
Other listed variants
- rs366597
- rs448281
- rs891189
- rs930072
- rs1622132
- rs1864213
- rs2301066
- rs2562582
- rs3776563
- rs3776566
- rs3776578
- rs3776583
- rs4869682
- rs4869685
- rs7726798
- rs7728680
- rs10941309
- rs11748249
- rs17368246
- rs60115512
- rs62354632
- rs72732544
- rs74321267
- rs74948768
- rs75096272
- rs77922630
- rs78813041
- rs78992973
- rs79029484
- rs79104438
- rs113100583
- rs115172522
- rs116126990
- rs146681673
- rs181358295
- rs192627549
- rs199787096
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.