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Variant (rsID / SNP)

rs201420791

ACADS

rs201420791 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACADS. Location: chromosome 12, position 121,176,322. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ACADSBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
12:121176322
Cytoband
12q24.31
HGVS
NM_000017.4(ACADS):c.796-14G>C
Allele change
Silent

Associated conditions / phenotypes

Deficiency of butyryl-CoA dehydrogenase

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.