Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57520
Gene Symbol: HECW2
HECW2 		0.700 GeneticVariation disease UNIPROT De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779 2017
Entrez Id: 57520
Gene Symbol: HECW2
HECW2 		0.700 Biomarker disease GENOMICS_ENGLAND De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779 2017
Entrez Id: 57520
Gene Symbol: HECW2
HECW2 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in HECW2 are associated with intellectual disability and epilepsy. 27334371 2016
Entrez Id: 57520
Gene Symbol: HECW2
HECW2 		0.700 Biomarker disease CTD_human
Entrez Id: 57520
Gene Symbol: HECW2
HECW2 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 57520
Gene Symbol: HECW2
HECW2 		0.700 CausalMutation disease CLINVAR