Gene entry
CTRC
chymotrypsin C
- Chromosome
- 1
- Cytoband
- 1p36.21
- Variants (rsID)
- 11
CTRC is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.21). Its official name is “chymotrypsin C”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs41307798Benignsingle nucleotide variantHereditary pancreatitis|Inborn genetic diseases
- rs121909293Conflicting interpretationssingle nucleotide variantPancreatitis, chronic, susceptibility to|Hereditary pancreatitis|Inborn genetic diseases
- rs140993290Conflicting interpretationssingle nucleotide variantHereditary pancreatitis|Inborn genetic diseases
- rs142560329Conflicting interpretationssingle nucleotide variantHereditary pancreatitis
- rs200678111Conflicting interpretationssingle nucleotide variantHereditary pancreatitis
- rs202058123Conflicting interpretationssingle nucleotide variantHereditary pancreatitis
- rs121909294Pathogenicsingle nucleotide variantPancreatitis, chronic, susceptibility to|Hereditary pancreatitis
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.