Variant (rsID / SNP)

rs111033750

rs111033750 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALT. Location: chromosome 9, position 34,648,433. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

GALTLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:34648433
Cytoband: 9p13.3
HGVS: NM_000155.4(GALT):c.667C>A (p.Arg223Ser)
Allele change: Missense_R114S

Associated conditions / phenotypes

Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase

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.