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Variant (rsID / SNP)

rs6336

NTRK1

rs6336 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NTRK1. Location: chromosome 1, position 156,848,918. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

NTRK1Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
1:156848918
Cytoband
1q23.1
HGVS
NM_002529.4(NTRK1):c.1810C>T (p.His604Tyr)
Allele change
Missense_H568Y

Associated conditions / phenotypes

Familial medullary thyroid carcinoma|Hereditary insensitivity to pain with anhidrosis

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.