Gene entry
SLC45A2
solute carrier family 45 member 2
- Chromosome
- 5
- Cytoband
- 5p13.2
- Variants (rsID)
- 23
SLC45A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5p13.2). Its official name is “solute carrier family 45 member 2”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs16891982Benignsingle nucleotide variantSkin/hair/eye pigmentation, variation in, 5|Malignant melanoma of skin
- rs2287949Benignsingle nucleotide variantOculocutaneous albinism type 4
- rs371152353Conflicting interpretationssingle nucleotide variantOculocutaneous albinism type 4
- rs121912621Pathogenicsingle nucleotide variantOculocutaneous albinism type 4
- rs387906317PathogenicDeletionOculocutaneous albinism type 4
- rs121912619Uncertain significancesingle nucleotide variantOculocutaneous albinism type 4
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.