Variant (rsID / SNP)
rs9549564
rs9549564 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP11A. Location: chromosome 13, position 113,479,813. The table records no clinical significance for this variant.
Reference-table entries
ATP11ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 13:113479813
- HGVS
- NM_032189.4,c.942G>A,p.Leu314Leu
- Allele change
- Synonymous_L314L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.