Variant (rsID / SNP)
rs1290177
rs1290177 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP11A. Location: chromosome 13, position 113,536,132. The table records no clinical significance for this variant.
Reference-table entries
ATP11ANot classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 13:113536132
- HGVS
- NM_032189.4,c.3330T>C,p.Asn1110Asn
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.