Variant (rsID / SNP)

rs771489305

rs771489305 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALC. Location: chromosome 14, position 88,414,089. Clinical significance in the table: Pathogenic.

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Reference-table entries

GALCPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 14:88414089
Cytoband: 14q31.3
HGVS: NM_000153.4(GALC):c.1472del (p.Lys491fs)

Associated conditions / phenotypes

Galactosylceramide beta-galactosidase deficiency

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.