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Variant (rsID / SNP)

rs140852621

NTRK1

rs140852621 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NTRK1. Location: chromosome 1, position 156,849,913. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NTRK1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:156849913
Cytoband
1q23.1
HGVS
NM_002529.4(NTRK1):c.2169C>T (p.Tyr723=)
Allele change
Synonymous_Y687Y

Associated conditions / phenotypes

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.