Variant (rsID / SNP)
rs2300455
rs2300455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACACB. Location: chromosome 12, position 109,623,516. The table records no clinical significance for this variant.
Reference-table entries
ACACBNot classified
- Variant type
- missense_variant
- Chromosome / position
- 12:109623516
- HGVS
- NM_001093.4,c.1951G>A,p.Ala651Thr
- Allele change
- Missense_A651T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.