Variant (rsID / SNP)
rs4911163
rs4911163 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACSS2. Location: chromosome 20, position 33,470,694. The table records no clinical significance for this variant.
Reference-table entries
ACSS2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:33470694
- HGVS
- NM_001076552.3,c.276C>T,p.Phe92Phe
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.