Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1447956961
rs1447956961
0.010 GeneticVariation BEFREE The human mitochondrial ND1/3460 mutation changes Ala52 to Thr in the ND1 subunit of Complex I, and causes Leber's hereditary optic neuropathy (LHON) [Huoponen et al.(1991) Am.J. Hum.Genet.48, 1147]. 9718301

1998