RS121908003 ACADS

Health Risk Chr 12:120727114 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Deficiency of butyryl-CoA dehydrogenase
ACADS-related disorder
Inborn genetic diseases
Deficiency of butyryl-CoA dehydrogenase
ACADS-related disorder
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
100%
1kG AMR
0.1%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in ACADS
rs61732144 rs121908004 rs57443665 rs28940872 rs387906308 rs28940874 rs121908006 rs28941773 rs28940875 rs147442301
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