Variant (rsID / SNP)
rs9204
rs9204 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACADS. Location: chromosome 12, position 121,177,778. Clinical significance in the table: Benign.
Reference-table entries
ACADSBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:121177778
- Cytoband
- 12q24.31
- HGVS
- NM_000017.4(ACADS):c.*527A>G
- 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.