Variant (rsID / SNP)

rs79677613

rs79677613 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACOX1. Location: chromosome 17, position 73,949,555. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ACOX1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:73949555
Cytoband: 17q25.1
HGVS: NM_004035.7(ACOX1):c.921G>A (p.Arg307=)
Allele change: Synonymous_R307R

Associated conditions / phenotypes

Acyl-CoA oxidase deficiency

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.