Variant (rsID / SNP)

rs3916

rs3916 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACADS. Location: chromosome 12, position 121,177,272. Clinical significance in the table: Benign.

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Reference-table entries

ACADSBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:121177272
Cytoband: 12q24.31
HGVS: NM_000017.4(ACADS):c.*21G>C
Allele change: Silent

Associated conditions / phenotypes

Deficiency of butyryl-CoA dehydrogenase

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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