Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555703272
rs1555703272
T 0.700 GeneticVariation CLINVAR SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency. 29211846

2018

dbSNP: rs377619533
rs377619533
A 0.700 GeneticVariation CLINVAR

dbSNP: rs201431517
rs201431517
A 0.700 CausalMutation CLINVAR