Gene entry
RFT1
RFT1 glycolipid translocator homolog
- Chromosome
- 3
- Cytoband
- 3p21.1
- Variants (rsID)
- 17
RFT1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p21.1). Its official name is “RFT1 glycolipid translocator homolog”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs140603849Benignsingle nucleotide variantRFT1-congenital disorder of glycosylation
- rs2564921Benignsingle nucleotide variantRFT1-congenital disorder of glycosylation
- rs35221142Benignsingle nucleotide variantRFT1-congenital disorder of glycosylation
- rs118203913Pathogenicsingle nucleotide variantRFT1-congenital disorder of glycosylation
- rs143232904Uncertain significancesingle nucleotide variantRFT1-congenital disorder of glycosylation
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.