Gene: CWF19L1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1 		0.600 Biomarker disease GENOMICS_ENGLAND Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability. 30167849 2018
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1 		0.600 Biomarker disease GENOMICS_ENGLAND Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy. 26197978 2016
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1 		0.600 GermlineCausalMutation disease ORPHANET Homozygous splice mutation in CWF19L1 in a Turkish family with recessive ataxia syndrome. 25361784 2014
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1 		0.600 CausalMutation disease CLINVAR
Entrez Id: 55280
Gene Symbol: CWF19L1
CWF19L1 		0.600 GeneticVariation disease CLINVAR