Gene entry
STRA6
signaling receptor and transporter of retinol STRA6
- Chromosome
- 15
- Cytoband
- 15q24.1
- Variants (rsID)
- 14
STRA6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q24.1). Its official name is “signaling receptor and transporter of retinol STRA6”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs145614612Benignsingle nucleotide variantMatthew-Wood syndrome
- rs736118Benignsingle nucleotide variantMatthew-Wood syndrome
- rs150814749Conflicting interpretationssingle nucleotide variantMatthew-Wood syndrome
- rs118203962Pathogenicsingle nucleotide variantMatthew-Wood syndrome
- rs118203959Uncertain significancesingle nucleotide variantMatthew-Wood 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.