Variant (rsID / SNP)
rs111033658
rs111033658 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALT. Location: chromosome 9, position 34,647,202. Clinical significance in the table: Pathogenic.
Reference-table entries
GALTPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:34647202
- Cytoband
- 9p13.3
- HGVS
- NM_000155.4(GALT):c.199C>T (p.Arg67Cys)
- Allele change
- Silent
Associated conditions / phenotypes
Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase|Galactosemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.