Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8802
Gene Symbol: SUCLG1
SUCLG1 		0.020 GeneticVariation disease BEFREE Expanding the phenotypic spectrum of Succinyl-CoA ligase deficiency through functional validation of a new SUCLG1 variant. 27484306 2016
Entrez Id: 8802
Gene Symbol: SUCLG1
SUCLG1 		0.020 GeneticVariation disease BEFREE Succinyl-CoA ligase deficiency due to an SUCLG1 mutation is a new cause for mitochondrial hepatoencephalomyopathy. 20453710 2010
Entrez Id: 8803
Gene Symbol: SUCLA2
SUCLA2 		0.010 GeneticVariation disease BEFREE Further studies are warranted to explore the mechanisms underlying the effects of the combination of XDH (p.Asn1109Thr) and SUCLA2 (199Ser) on thiopurine-induced leukopenia. 26863601 2016
Entrez Id: 7498
Gene Symbol: XDH
XDH 		0.010 GeneticVariation disease BEFREE Further studies are warranted to explore the mechanisms underlying the effects of the combination of XDH (p.Asn1109Thr) and SUCLA2 (199Ser) on thiopurine-induced leukopenia. 26863601 2016