Variant (rsID / SNP)

rs16852179

rs16852179 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACAD9. Location: chromosome 3, position 128,627,999. Clinical significance in the table: Benign.

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Reference-table entries

ACAD9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:128627999
Cytoband: 3q21.3
HGVS: NM_014049.5(ACAD9):c.1485+57T>C
Allele change: Silent

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.