Gene entry
FLVCR2
FLVCR choline and putative heme transporter 2
- Chromosome
- 14
- Cytoband
- 14q24.3
- Variants (rsID)
- 20
FLVCR2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q24.3). Its official name is “FLVCR choline and putative heme transporter 2”. The reference table lists 20 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs267606825Pathogenicsingle nucleotide variantFowler syndrome
- rs193042691Uncertain significancesingle nucleotide variantPosterior column ataxia-retinitis pigmentosa syndrome
- rs267606823Uncertain significancesingle nucleotide variantFowler syndrome|Posterior column ataxia-retinitis pigmentosa 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.