Variant (rsID / SNP)
rs5030856
rs5030856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAH. Location: chromosome 12, position 103,237,454. Clinical significance in the table: Pathogenic.
Reference-table entries
PAHPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:103237454
- Cytoband
- 12q23.2
- HGVS
- NM_000277.3(PAH):c.1169A>G (p.Glu390Gly)
- Allele change
- Missense_E390G
Associated conditions / phenotypes
Hyperphenylalaninemia|Phenylketonuria
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.