Variant (rsID / SNP)

rs17198

rs17198 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALC. Location: chromosome 14, position 88,399,488. Clinical significance in the table: Benign.

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Reference-table entries

GALCBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:88399488
Cytoband: 14q31.3
HGVS: NM_000153.4(GALC):c.*1588T>G
Allele change: Silent

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.