Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Indifference to Pain, Congenital, Autosomal Recessive
0.700 CausalMutation CLINVAR Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations. 17470132 2007
Indifference to Pain, Congenital, Autosomal Recessive
0.700 CausalMutation CLINVAR An SCN9A channelopathy causes congenital inability to experience pain. 17167479 2006