Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398123064
rs398123064
0.010 GeneticVariation BEFREE Our group has previously identified the <i>GBA2</i> c.1780G>C [p.Asp594His] missense mutation, in a Cypriot consanguineous family with spastic ataxia. 30308956

2018