Gene entry
SLC19A1
solute carrier family 19 member 1
- Chromosome
- 21
- Cytoband
- 21q22.3
- Variants (rsID)
- 42
SLC19A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 21 (region 21q22.3). Its official name is “solute carrier family 19 member 1”. The reference table lists 42 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
Other listed variants
- rs7867
- rs914232
- rs944422
- rs1051296
- rs1051298
- rs1475596
- rs2236483
- rs2838952
- rs2838956
- rs3753019
- rs3788189
- rs3788205
- rs4818789
- rs7278425
- rs11089010
- rs12483377
- rs13050920
- rs60881836
- rs62214272
- rs73228786
- rs73228800
- rs77326997
- rs79091853
- rs112637375
- rs112864061
- rs114130583
- rs116618591
- rs117417101
- rs117473978
- rs118066876
- rs118127630
- rs144147445
- rs189383130
- rs199792935
- rs367664040
- rs544415768
- rs557154056
- rs560066114
- rs576935158
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.