Gene entry
SLC7A14
solute carrier family 7 member 14
- Chromosome
- 3
- Cytoband
- 3q26.2
- Variants (rsID)
- 36
SLC7A14 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q26.2). Its official name is “solute carrier family 7 member 14”. The reference table lists 36 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs2276717Benignsingle nucleotide variantRetinitis pigmentosa 68
Other listed variants
- rs759712
- rs1468977
- rs1861939
- rs1861940
- rs2052397
- rs2287489
- rs4955730
- rs6799974
- rs7651111
- rs9290392
- rs9828037
- rs10513683
- rs10936636
- rs11719718
- rs11915263
- rs34322079
- rs55977230
- rs62293556
- rs62294671
- rs63156262
- rs73040372
- rs78577578
- rs114883808
- rs114994163
- rs115729600
- rs116040996
- rs116862087
- rs142416793
- rs181011740
- rs182823777
- rs189535853
- rs190070175
- rs202144632
- rs369598601
- rs371214263
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.