RS113994169 ACADVL
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What This Variant Does
"[OMIM:?]
Associated Conditions
Very long chain acyl-CoA dehydrogenase deficiency
Inborn genetic diseases
Very long chain acyl-CoA dehydrogenase deficiency
Very long chain acyl-CoA dehydrogenase deficiency
Inborn genetic diseases
Very long chain acyl-CoA dehydrogenase deficiency
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
99.9%
1kG EUR
100%
1kG SAS
100%
Other Variants in ACADVL