Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 407973
Gene Symbol: SCA20
SCA20 		0.300 GermlineCausalMutation disease ORPHANET
Entrez Id: 57231
Gene Symbol: SNX14
SNX14 		0.010 GeneticVariation disease BEFREE SNX14 mutations affect endoplasmic reticulum-associated neutral lipid metabolism in autosomal recessive spinocerebellar ataxia 20. 29635513 2018