Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7518
Gene Symbol: XRCC4
XRCC4 		0.600 Biomarker disease GENOMICS_ENGLAND Mitochondrial medicine in the omics era. 29903433 2018
Entrez Id: 7518
Gene Symbol: XRCC4
XRCC4 		0.600 GeneticVariation disease UNIPROT XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency. 26255102 2015
Entrez Id: 7518
Gene Symbol: XRCC4
XRCC4 		0.600 GeneticVariation disease UNIPROT Mutations in the NHEJ component XRCC4 cause primordial dwarfism. 25728776 2015
Entrez Id: 7518
Gene Symbol: XRCC4
XRCC4 		0.600 GeneticVariation disease UNIPROT Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability. 25839420 2015
Entrez Id: 7518
Gene Symbol: XRCC4
XRCC4 		0.600 GeneticVariation disease UNIPROT Genomic analysis of primordial dwarfism reveals novel disease genes. 24389050 2014
Entrez Id: 7518
Gene Symbol: XRCC4
XRCC4 		0.600 Biomarker disease GENOMICS_ENGLAND Genomic analysis of primordial dwarfism reveals novel disease genes. 24389050 2014
Entrez Id: 7518
Gene Symbol: XRCC4
XRCC4 		0.600 CausalMutation disease CLINVAR