Disease: HSAN Type IV ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs914061514
rs914061514
Entrez Id: 4914
Gene Symbol: NTRK1
NTRK1
CUI: C0020074
Disease:
HSAN Type IV 		C 0.700 GeneticVariation CLINVAR Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation. 19651702 2009
dbSNP: rs914061514
rs914061514
Entrez Id: 4914
Gene Symbol: NTRK1
NTRK1
CUI: C0020074
Disease:
HSAN Type IV 		C 0.700 GeneticVariation CLINVAR Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis. 8696348 1996
dbSNP: rs914061514
rs914061514
Entrez Id: 4914
Gene Symbol: NTRK1
NTRK1
CUI: C0020074
Disease:
HSAN Type IV 		C 0.700 CausalMutation CLINVAR