Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs891954464
rs891954464
Entrez Id: 3032
Gene Symbol: HADHB
HADHB
CUI: C1969443
Disease:
Trifunctional Protein Deficiency With Myopathy And Neuropathy
0.800 GeneticVariation UNIPROT
dbSNP: rs891954464
rs891954464
Entrez Id: 3032
Gene Symbol: HADHB
HADHB
CUI: C1969443
Disease:
Trifunctional Protein Deficiency With Myopathy And Neuropathy
C 0.800 GeneticVariation CLINVAR