Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514262
rs397514262
ERBB4
0.800 GeneticVariation UNIPROT ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19. 24119685

2013
dbSNP: rs397514262
rs397514262
ERBB4
T 0.800 CausalMutation CLINVAR