Gene entry
FRRS1L
ferric chelate reductase 1 like
- Chromosome
- 9
- Cytoband
- 9q31.3
- Variants (rsID)
- 11
FRRS1L is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q31.3). Its official name is “ferric chelate reductase 1 like”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs149005559Likely benignsingle nucleotide variantDevelopmental and epileptic encephalopathy, 37
- rs878853282PathogenicDeletionDevelopmental and epileptic encephalopathy, 37|Seizure|Chorea|Progressive encephalopathy
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.