Variant (rsID / SNP)
rs2303963
rs2303963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPRB. Location: chromosome 12, position 70,953,277. The table records no clinical significance for this variant.
Reference-table entries
PTPRBNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:70953277
- HGVS
- NM_001109754.4,c.4560A>G,p.Ala1520Ala
- Allele change
- Synonymous_A1520A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.