Variant (rsID / SNP)

rs118204429

rs118204429 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDOB. Location: chromosome 9, position 104,192,183. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

ALDOBPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:104192183
Cytoband: 9q31.1
HGVS: NM_000035.4(ALDOB):c.178C>T (p.Arg60Ter)
Allele change: Nonsense_R60X

Associated conditions / phenotypes

Hereditary fructosuria|See cases

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.