Variant (rsID / SNP)

rs76212747

rs76212747 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAH. Location: chromosome 12, position 103,246,701. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PAHPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 12:103246701
Cytoband: 12q23.2
HGVS: NM_000277.3(PAH):c.734T>C (p.Val245Ala)
Allele change: Missense_V245A

Associated conditions / phenotypes

Hyperphenylalaninemia|Phenylketonuria

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.