Variant (rsID / SNP)
rs2532060
rs2532060 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPP1R12C. Location: chromosome 19, position 55,614,923. The table records no clinical significance for this variant.
Reference-table entries
PPP1R12CNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:55614923
- HGVS
- NM_017607.4,c.585A>G,p.Glu195Glu
- Allele change
- Synonymous_E195E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.