Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398124646
rs398124646
EHHADH ; MIR5588
CUI: C3810100
Disease: FANCONI RENOTUBULAR SYNDROME 3
FANCONI RENOTUBULAR SYNDROME 3 		0.800 GeneticVariation UNIPROT Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome. 24401050

2014
dbSNP: rs398124646
rs398124646
EHHADH ; MIR5588
CUI: C3810100
Disease: FANCONI RENOTUBULAR SYNDROME 3
FANCONI RENOTUBULAR SYNDROME 3 		T 0.800 CausalMutation CLINVAR