Variant (rsID / SNP)
rs2252784
rs2252784 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPRB. Location: chromosome 12, position 71,002,893. The table records no clinical significance for this variant.
Reference-table entries
PTPRBNot classified
- Variant type
- missense_variant
- Chromosome / position
- 12:71002893
- HGVS
- NM_001109754.4,c.935G>A,p.Arg312Lys
- Allele change
- Missense_R312K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.