rs74315322, HAX1

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Severe congenital neutropenia
CUI: C1853118
Disease: Severe congenital neutropenia
0.700 CausalMutation CLINVAR
nervous system disorder
CUI: C0027765
Disease: nervous system disorder
0.010 GeneticVariation BEFREE All the three patients with Q190X mutations who were alive and available for evaluation developed neurological disease with decreased cognitive function, and three of four patients who reached 10 years developed epilepsy. 18513342 2008
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.010 GeneticVariation BEFREE All the three patients with Q190X mutations who were alive and available for evaluation developed neurological disease with decreased cognitive function, and three of four patients who reached 10 years developed epilepsy. 18513342 2008