Variant (rsID / SNP)

rs13434465

rs13434465 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACOX3. Location: chromosome 4, position 8,390,948. Clinical significance in the table: Benign.

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Reference-table entries

ACOX3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:8390948
Cytoband: 4p16.1
HGVS: NM_003501.3(ACOX3):c.1489G>A (p.Asp497Asn)
Allele change: Missense_D497N

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.