Gene entry
RFX6
regulatory factor X6
- Chromosome
- 6
- Cytoband
- 6q22.1
- Variants (rsID)
- 19
RFX6 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q22.1). Its official name is “regulatory factor X6”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs4946206Benignsingle nucleotide variant
- rs77146142Benignsingle nucleotide variantMonogenic diabetes|Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome
- rs146081967Conflicting interpretationssingle nucleotide variantMonogenic diabetes
- rs146115506Conflicting interpretationssingle nucleotide variantMonogenic diabetes
- rs57924353Likely benignsingle nucleotide variantMonogenic diabetes
- rs144648002Pathogenicsingle nucleotide variantHypoplastic pancreas-intestinal atresia-hypoplastic gallbalder 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.