Variant (rsID / SNP)

rs104894845

rs104894845 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLA. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GLAConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Cytoband: Xq22.1
HGVS: NM_000169.3(GLA):c.427G>A (p.Ala143Thr)
Allele change: Silent

Associated conditions / phenotypes

Fabry disease|Cardiomyopathy|Cardiovascular phenotype|Primary familial hypertrophic cardiomyopathy

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.