Gene entry
GNB1
G protein subunit beta 1
- Chromosome
- 1
- Cytoband
- 1p36.33
- Variants (rsID)
- 8
GNB1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.33). Its official name is “G protein subunit beta 1”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs752746786Pathogenicsingle nucleotide variantInborn genetic diseases|7 conditions|13 conditions|Intellectual disability, autosomal dominant 42|Myelodysplastic syndrome|Neurodevelopmental Disability|Hypotonia|Seizure|LEUKEMIA, CHRONIC LYMPHOCYTIC, SOMATIC|Neurodevelopmental disorder|Global developmental delay|Neurodevelopmental abnormality|Intellectual disability|Cerebral palsy|Neurodevelopmental delay
- rs869312825Pathogenicsingle nucleotide variant10 conditions|Intellectual disability, autosomal dominant 42|Hypotonia|Seizure|Neurodevelopmental Disability
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.