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Variant (rsID / SNP)

rs190921137

GALC

rs190921137 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALC. Location: chromosome 14, position 88,431,885. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GALCConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
14:88431885
Cytoband
14q31.3
HGVS
NM_000153.4(GALC):c.997G>A (p.Gly333Arg)
Allele change
Missense_G310R

Associated conditions / phenotypes

Galactosylceramide beta-galactosidase deficiency

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.