Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6572
Gene Symbol: SLC18A3
SLC18A3 		0.600 Biomarker disease GENOMICS_ENGLAND SLC18A3 variants lead to fetal akinesia deformation sequence early in pregnancy. 31059209 2019
Entrez Id: 6572
Gene Symbol: SLC18A3
SLC18A3 		0.600 GeneticVariation disease UNIPROT Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. 27590285 2016
Entrez Id: 6572
Gene Symbol: SLC18A3
SLC18A3 		0.600 Biomarker disease GENOMICS_ENGLAND Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. 27590285 2016
Entrez Id: 6572
Gene Symbol: SLC18A3
SLC18A3 		0.600 CausalMutation disease CLINVAR
Entrez Id: 1103
Gene Symbol: CHAT
CHAT 		0.100 CausalMutation disease CLINVAR