Gene: ND6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4541
Gene Symbol: ND6
ND6 		0.110 GeneticVariation phenotype BEFREE Representative of these mutations is a heteroplasmic mutation in MTND6 at np 14459 whose clinical presentations range from adult-onset blindness to pediatric dystonia and basal ganglial degeneration. 8090716 1994
Entrez Id: 4541
Gene Symbol: ND6
ND6 		0.110 GeneticVariation phenotype CLINVAR