Gene: SPTBN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6712
Gene Symbol: SPTBN2
SPTBN2 		0.010 GeneticVariation disease BEFREE Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia. 31066025 2019