Gene entry
NODAL
nodal growth differentiation factor
- Chromosome
- 10
- Cytoband
- 10q22.1
- Variants (rsID)
- 10
NODAL is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q22.1). Its official name is “nodal growth differentiation factor”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs1904589Benignsingle nucleotide variantHoloprosencephaly sequence|Visceral heterotaxy 5, autosomal
- rs2279253Benignsingle nucleotide variantVisceral heterotaxy 5, autosomal|Holoprosencephaly sequence
- rs121909283Conflicting interpretationssingle nucleotide variantVisceral heterotaxy 5, autosomal|Inborn genetic diseases|Wolff-Parkinson-White pattern|Visceral heterotaxy
- rs150819707Conflicting interpretationssingle nucleotide variantVisceral heterotaxy 5, autosomal|Holoprosencephaly sequence
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.
