Variant (rsID / SNP)
rs2228945
rs2228945 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRKCA. Location: chromosome 17, position 64,785,022. The table records no clinical significance for this variant.
Reference-table entries
PRKCANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:64785022
- HGVS
- NM_002737.3,c.1779G>A,p.Glu593Glu
- Allele change
- Synonymous_E593E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.