RS137852769 HADHA

Health Risk Chr 2:26195184
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mitochondrial trifunctional protein deficiency
LCHAD deficiency with maternal acute fatty liver of pregnancy
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Inborn genetic diseases
HADHA-related disorder
Mitochondrial trifunctional protein deficiency 1
Metabolic disease
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Mitochondrial trifunctional protein deficiency
HADHA-related disorder
Mitochondrial trifunctional protein deficiency
LCHAD deficiency with maternal acute fatty liver of pregnancy
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Inborn genetic diseases
HADHA-related disorder
GWAS Studies (3)
Trait Risk Allele OR / Beta P-value Study
X-16580 levels C OR: 0.89 2E-12 PubMed
3-hydroxylaurate levels C OR: 0.77 9E-10 PubMed
3-hydroxydecanoate levels C OR: 0.64 5E-7 PubMed
Other Variants in HADHA
rs137852770 rs786205088 rs781222705 rs137852771 rs1574600309 rs137852772 rs137852774 rs137852775 rs147103714 rs749848370
Ask Dr. Hemsworth about this variant