Gene: NTRK1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1026300967
rs1026300967
NTRK1
C 0.700 GeneticVariation CLINVAR A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV). 27676246

2017
dbSNP: rs1026300967
rs1026300967
NTRK1
C 0.700 GeneticVariation CLINVAR Novel 9 amino acid in-frame deletion in the NTRK1 tyrosine kinase domain in a patient with congenital insensitivity to pain with anhydrosis. 28940190

2017
dbSNP: rs1553263326
rs1553263326
NTRK1
A 0.700 GeneticVariation CLINVAR A Comprehensive Functional Analysis of NTRK1 Missense Mutations Causing Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN IV). 27676246

2017
dbSNP: rs1553263326
rs1553263326
NTRK1
A 0.700 GeneticVariation CLINVAR Novel 9 amino acid in-frame deletion in the NTRK1 tyrosine kinase domain in a patient with congenital insensitivity to pain with anhydrosis. 28940190

2017
dbSNP: rs1026300967
rs1026300967
NTRK1
C 0.700 GeneticVariation CLINVAR Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort. 22302274

2012
dbSNP: rs1553263326
rs1553263326
NTRK1
A 0.700 GeneticVariation CLINVAR Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort. 22302274

2012