Variant (rsID / SNP)
rs61754215
rs61754215 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPRG. Location: chromosome 3, position 62,180,792. The table records no clinical significance for this variant.
Reference-table entries
PTPRGNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 3:62180792
- HGVS
- NM_002841.4,c.1275C>T,p.Ala425Ala
- Allele change
- Synonymous_A425A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.