Gene entry
FOLR1
folate receptor alpha
- Chromosome
- 11
- Cytoband
- 11q13.4
- Variants (rsID)
- 11
FOLR1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q13.4). Its official name is “folate receptor alpha”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs139633601Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder|Cerebral folate transport deficiency
- rs143413500Conflicting interpretationssingle nucleotide variantHistory of neurodevelopmental disorder|Cerebral folate transport deficiency
- rs144637717Conflicting interpretationssingle nucleotide variantCerebral folate transport deficiency|History of neurodevelopmental disorder|Seizure
- rs375444839Conflicting interpretationssingle nucleotide variantCerebral folate transport deficiency
- rs564331848Conflicting interpretationssingle nucleotide variantCerebral folate transport deficiency
- rs755278391Conflicting interpretationssingle nucleotide variantCerebral folate transport deficiency|History of neurodevelopmental disorder
- rs76191655Conflicting interpretationssingle nucleotide variantCerebral folate transport deficiency|History of neurodevelopmental disorder
- rs886042924Conflicting interpretationssingle nucleotide variantCerebral folate transport deficiency
- rs121918405Pathogenicsingle nucleotide variantCerebral folate transport deficiency
- rs147155003Uncertain significancesingle nucleotide variantCerebral folate transport deficiency
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.