Disease: Pain ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs769854785
rs769854785
Entrez Id: 4914
Gene Symbol: NTRK1
NTRK1
CUI: C0030193
Disease:
Pain 		0.010 GeneticVariation BEFREE Recently, a missense point mutation was found in the NGFB gene (C661T, leading to the aminoacid substitution R100W) of individuals affected by a form of hereditary loss of pain perception (hereditary sensory and autonomic neuropathy type V, HSAN V). 19945432 2010