Variant (rsID / SNP)

rs1800601

rs1800601 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NTRK1. Location: chromosome 1, position 156,785,617. Clinical significance in the table: Benign.

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Reference-table entries

NTRK1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:156785617
Cytoband: 1q23.1
HGVS: NM_003975.4(SH2D2A):c.123+181C>T
Allele change: Silent

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.