Gene entry
SLC24A2
solute carrier family 24 member 2
- Chromosome
- 9
- Cytoband
- 9p22.1-p21.3
- Variants (rsID)
- 210
SLC24A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p22.1-p21.3). Its official name is “solute carrier family 24 member 2”. The reference table lists 210 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs61745273Benignsingle nucleotide variantAbnormal retinal morphology
Other listed variants
- rs224025
- rs415026
- rs713168
- rs717081
- rs722991
- rs752539
- rs882123
- rs1003173
- rs1006240
- rs1031602
- rs1156645
- rs1182653
- rs1182656
- rs1182659
- rs1182665
- rs1182672
- rs1327404
- rs1333775
- rs1409955
- rs1413254
- rs1456961
- rs1536517
- rs1551534
- rs1591219
- rs1885232
- rs1889245
- rs2039459
- rs2039460
- rs2039461
- rs2124836
- rs2154091
- rs2208553
- rs2209798
- rs2383103
- rs2383122
- rs2383134
- rs3780217
- rs3837225
- rs4246835
- rs4258076
- rs4531135
- rs4556171
- rs4977233
- rs4977303
- rs4977334
- rs4977370
- rs4977371
- rs4977384
- rs4977386
- rs4977390
- rs4977400
- rs4977404
- rs4977544
- rs4977547
- rs6475389
- rs7018634
- rs7019685
- rs7021788
- rs7026700
- rs7029347
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.