Variant (rsID / SNP)
rs3796403
rs3796403 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP2R2C. Location: chromosome 4, position 6,325,086. The table records no clinical significance for this variant.
Reference-table entries
PPP2R2CNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:6325086
- HGVS
- NM_020416.4,c.1287C>T,p.Ile429Ile
- Allele change
- Synonymous_I415I
Associated conditions / phenotypes
Synonymous_I429I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.