Variant (rsID / SNP)
rs121918466
rs121918466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTPN11. Location: chromosome 12, position 112,888,220. Clinical significance in the table: Pathogenic.
Reference-table entries
PTPN11Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:112888220
- Cytoband
- 12q24.13
- HGVS
- NM_002834.5(PTPN11):c.236A>G (p.Gln79Arg)
- Allele change
- Missense_Q79R
Associated conditions / phenotypes
Noonan syndrome 1|RASopathy|Noonan syndrome|LEOPARD syndrome 1|Metachondromatosis|Juvenile myelomonocytic leukemia|Noonan syndrome 1|Noonan syndrome 3|Noonan syndrome and Noonan-related syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.