Gene entry
SLC29A3
solute carrier family 29 member 3
- Chromosome
- 10
- Cytoband
- 10q22.1
- Variants (rsID)
- 26
SLC29A3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q22.1). Its official name is “solute carrier family 29 member 3”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
13 reference-table entries with clinical significance.
- rs1084004Benignsingle nucleotide variantH syndrome
- rs148092033Benignsingle nucleotide variantH syndrome
- rs2277257Benignsingle nucleotide variantH syndrome
- rs77339410Benignsingle nucleotide variantH syndrome
- rs780668Benignsingle nucleotide variantH syndrome|Gemcitabine response|Acanthosis nigricans
- rs746408350Conflicting interpretationssingle nucleotide variantH syndrome
- rs2275579Likely benignsingle nucleotide variantH syndrome
- rs267607056Likely pathogenicsingle nucleotide variantH syndrome
- rs121912583Pathogenicsingle nucleotide variantH syndrome
- rs121912584Pathogenicsingle nucleotide variantH syndrome
- rs267607058Pathogenicsingle nucleotide variantH syndrome
- rs142216905Uncertain significancesingle nucleotide variantH syndrome
- rs201610819Uncertain significancesingle nucleotide variantH syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.