Variant (rsID / SNP)

rs55909005

rs55909005 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NTRK1. Location: chromosome 1, position 156,838,432. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NTRK1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:156838432
Cytoband: 1q23.1
HGVS: NM_002529.4(NTRK1):c.710C>T (p.Thr237Met)
Allele change: Missense_T207M

Associated conditions / phenotypes

Hereditary insensitivity to pain with anhidrosis

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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