Variant (rsID / SNP)
rs4103004
rs4103004 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PP2D1. Location: chromosome 3, position 20,042,834. The table records no clinical significance for this variant.
Reference-table entries
PP2D1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 3:20042834
- HGVS
- NM_001252657.2,c.778G>A,p.Ala260Thr
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.