Gene entry
NTRK1
neurotrophic receptor tyrosine kinase 1
- Chromosome
- 1
- Cytoband
- 1q23.1
- Variants (rsID)
- 28
NTRK1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q23.1). Its official name is “neurotrophic receptor tyrosine kinase 1”. The reference table lists 28 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs147438950Benignsingle nucleotide variantHereditary insensitivity to pain with anhidrosis
- rs1800601Benignsingle nucleotide variantHereditary insensitivity to pain with anhidrosis
- rs41267425Benignsingle nucleotide variantHereditary insensitivity to pain with anhidrosis
- rs55909005Benignsingle nucleotide variantHereditary insensitivity to pain with anhidrosis
- rs6336Benignsingle nucleotide variantFamilial medullary thyroid carcinoma|Hereditary insensitivity to pain with anhidrosis
- rs6339Benignsingle nucleotide variantFamilial medullary thyroid carcinoma|Hereditary insensitivity to pain with anhidrosis
- rs137994522Conflicting interpretationssingle nucleotide variantFamilial medullary thyroid carcinoma|Hereditary insensitivity to pain with anhidrosis
- rs140852621Conflicting interpretationssingle nucleotide variantHereditary insensitivity to pain with anhidrosis
- rs186649954Conflicting interpretationssingle nucleotide variantHereditary insensitivity to pain with anhidrosis
- rs80356677Likely pathogenicsingle nucleotide variantHereditary insensitivity to pain with anhidrosis
- rs80356674Pathogenicsingle nucleotide variantHereditary insensitivity to pain with anhidrosis|Inborn genetic diseases
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.