Gene entry
SLC17A1
solute carrier family 17 member 1
- Chromosome
- 6
- Cytoband
- 6p22.2
- Variants (rsID)
- 34
SLC17A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p22.2). Its official name is “solute carrier family 17 member 1”. The reference table lists 34 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs1165196Not classifiedmissense_variantGout|Atrial Fibrillation|Hyperuricemia|Hypercholesterolemia, Familial, 1|Hypertriglyceridemia 1|Polycystic Kidney Disease|Hypercholesterolemia, Familial, 3|Hypertriglyceridemia, Transient Infantile|Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease|Enthesopathy
Other listed variants
- rs1165151
- rs1165198
- rs1165209
- rs1183201
- rs1185567
- rs1892253
- rs2154219
- rs2328893
- rs2762353
- rs3734526
- rs3922841
- rs4712969
- rs6910549
- rs6933573
- rs6940698
- rs7749149
- rs9358890
- rs9461212
- rs9461218
- rs11754288
- rs13200921
- rs16890978
- rs17268697
- rs17342717
- rs72843528
- rs73733698
- rs74521692
- rs76694514
- rs76788698
- rs78832046
- rs112544908
- rs183024672
- rs185235428
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.