Gene: ERCC8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1161
Gene Symbol: ERCC8
ERCC8 		0.110 GeneticVariation phenotype BEFREE Homozygosity mapping and whole exome sequencing reveal a novel ERCC8 mutation in a Chinese consanguineous family with unique cerebellar ataxia. 30871974 2019
Entrez Id: 1161
Gene Symbol: ERCC8
ERCC8 		0.110 CausalMutation phenotype CLINVAR