Variant (rsID / SNP)

rs118092776

rs118092776 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PAH. Location: chromosome 12, position 103,306,579. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PAHUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 12:103306579
Cytoband: 12q23.2
HGVS: NM_000277.3(PAH):c.158G>A (p.Arg53His)
Allele change: Missense_R53H

Associated conditions / phenotypes

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.