Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200725073
rs200725073
SLC25A46
0.800 GeneticVariation UNIPROT Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. 26168012

2015
dbSNP: rs1057518748
rs1057518748
SLC25A46
T 0.800 CausalMutation CLINVAR

dbSNP: rs1057518748
rs1057518748
SLC25A46
0.800 GeneticVariation UNIPROT

dbSNP: rs1057518750
rs1057518750
SLC25A46
0.800 GeneticVariation UNIPROT

dbSNP: rs1057518750
rs1057518750
SLC25A46
T 0.800 CausalMutation CLINVAR

dbSNP: rs200725073
rs200725073
SLC25A46
A 0.800 CausalMutation CLINVAR

dbSNP: rs746681765
rs746681765
SLC25A46
T 0.800 CausalMutation CLINVAR

dbSNP: rs746681765
rs746681765
SLC25A46
0.800 GeneticVariation UNIPROT

dbSNP: rs1057518749
rs1057518749
SLC25A46
GACTT 0.700 CausalMutation CLINVAR

dbSNP: rs1057519294
rs1057519294
SLC25A46
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057519295
rs1057519295
SLC25A46
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519296
rs1057519296
SLC25A46
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057519416
rs1057519416
SLC25A46 ; TMEM232
GC 0.700 CausalMutation CLINVAR

dbSNP: rs1184021143
rs1184021143
SLC25A46
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554093168
rs1554093168
SLC25A46
T 0.700 GeneticVariation CLINVAR