Variant (rsID / SNP)
rs2278911
rs2278911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CIP2A. Location: chromosome 3, position 108,298,260. The table records no clinical significance for this variant.
Reference-table entries
CIP2ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 3:108298260
- HGVS
- NM_020890.3,c.686G>A,p.Arg229Gln
- Allele change
- Missense_R229Q
Associated conditions / phenotypes
Prostate Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.