Gene entry
CHRNG
cholinergic receptor nicotinic gamma subunit
- Chromosome
- 2
- Cytoband
- 2q37.1
- Variants (rsID)
- 10
CHRNG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q37.1). Its official name is “cholinergic receptor nicotinic gamma subunit”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs2099489Benignsingle nucleotide variantAutosomal recessive multiple pterygium syndrome|Lethal multiple pterygium syndrome
- rs138125827Conflicting interpretationssingle nucleotide variantAutosomal recessive multiple pterygium syndrome|Lethal multiple pterygium syndrome
- rs143272752Conflicting interpretationssingle nucleotide variantAutosomal recessive multiple pterygium syndrome|Lethal multiple pterygium syndrome
- rs71421651Conflicting interpretationssingle nucleotide variantAutosomal recessive multiple pterygium syndrome|Lethal multiple pterygium syndrome
- rs75369104Conflicting interpretationssingle nucleotide variantAutosomal recessive multiple pterygium syndrome|Lethal multiple pterygium syndrome
- rs753990044Conflicting interpretationssingle nucleotide variantAutosomal recessive multiple pterygium syndrome
- rs767503038PathogenicDeletionLethal multiple pterygium syndrome|Autosomal recessive multiple pterygium syndrome|Inborn genetic diseases|CHRNG-Related Disorders|Abnormality of prenatal development or birth
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.