Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs281864934
rs281864934
CHMP2B
0.800 GeneticVariation UNIPROT Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS). 20352044

2010
dbSNP: rs281864934
rs281864934
CHMP2B
0.800 GeneticVariation UNIPROT ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B). 16807408

2006
dbSNP: rs281864934
rs281864934
CHMP2B
A 0.800 CausalMutation CLINVAR

dbSNP: rs63751126
rs63751126
CHMP2B
C 0.700 CausalMutation CLINVAR