RS113994167 ACADVL
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What This Variant Does
"[OMIM:?]
Associated Conditions
Very long chain acyl-CoA dehydrogenase deficiency
Inborn genetic diseases
See cases
ACADVL-related disorder
Acute rhabdomyolysis
Very long chain acyl-CoA dehydrogenase deficiency
Inborn genetic diseases
See cases
ACADVL-related disorder
Acute rhabdomyolysis
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Tetradecenoylcarnitine levels | — | OR: 1.57 | 1E-14 | PubMed |
Other Variants in ACADVL