Variant (rsID / SNP)

rs323893

rs323893 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACY1. Location: chromosome 3, position 52,020,411. Clinical significance in the table: Benign.

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Reference-table entries

ACY1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:52020411
Cytoband: 3p21.2
HGVS: NM_000666.3(ACY1):c.437-20C>T
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.