Variant (rsID / SNP)
rs3803036
rs3803036 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPRR. Location: chromosome 12, position 71,139,664. The table records no clinical significance for this variant.
Reference-table entries
PTPRRNot classified
- Variant type
- missense_variant
- Chromosome / position
- 12:71139664
- HGVS
- NM_002849.4,c.941A>G,p.Lys314Arg
- Allele change
- Silent
Associated conditions / phenotypes
Myopia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.