Gene entry
TYRP1
tyrosinase related protein 1
- Chromosome
- 9
- Cytoband
- 9p23
- Variants (rsID)
- 13
TYRP1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9p23). Its official name is “tyrosinase related protein 1”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs16929374Benignsingle nucleotide variantOculocutaneous albinism type 3
- rs683Benignsingle nucleotide variantOculocutaneous albinism type 3
- rs144041081Conflicting interpretationssingle nucleotide variantOculocutaneous albinism type 3
- rs147268542Conflicting interpretationssingle nucleotide variantOculocutaneous albinism type 3
- rs184910238Conflicting interpretationssingle nucleotide variant
- rs61752937Conflicting interpretationssingle nucleotide variantOculocutaneous albinism type 3
- rs61752939Conflicting interpretationssingle nucleotide variantOculocutaneous albinism type 3
- rs281865424Likely pathogenicsingle nucleotide variantOculocutaneous albinism type 3|Nonsyndromic Oculocutaneous Albinism
- rs104894130Pathogenicsingle nucleotide variantOCULOCUTANEOUS ALBINISM, TYPE II, MODIFIER OF|Oculocutaneous albinism type 3
- rs41303651Uncertain significancesingle nucleotide variant
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.