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Gene entry

GLA

galactosidase alpha

Chromosome
X
Cytoband
Xq22.1
Variants (rsID)
154

GLA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq22.1). Its official name is “galactosidase alpha”. The reference table lists 154 variants (rsID) for this gene.

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Clinically classified variants

151 reference-table entries with clinical significance.

  • rs3027584Benignsingle nucleotide variantFabry disease
  • rs3027589Benignsingle nucleotide variant
  • rs397515869Benignsingle nucleotide variantFabry disease
  • rs104894845Conflicting interpretationssingle nucleotide variantFabry disease|Cardiomyopathy|Cardiovascular phenotype|Primary familial hypertrophic cardiomyopathy
  • rs111422676Conflicting interpretationssingle nucleotide variantFabry disease
  • rs144994244Conflicting interpretationssingle nucleotide variantFabry disease
  • rs148158093Conflicting interpretationssingle nucleotide variantFabry disease|Cardiovascular phenotype|Cardiomyopathy
  • rs149391489Conflicting interpretationssingle nucleotide variantFabry disease|Cardiovascular phenotype
  • rs150547672Conflicting interpretationssingle nucleotide variantMigalastat response|Fabry disease|Cardiovascular phenotype|Cardiomyopathy
  • rs201449986Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy|Fabry disease
  • rs28935490Conflicting interpretationssingle nucleotide variantFabry disease|Sudden unexplained death|Cardiovascular phenotype|Hypertrophic cardiomyopathy|Cardiomyopathy
  • rs372416832Conflicting interpretationssingle nucleotide variantFabry disease
  • rs398123223Conflicting interpretationssingle nucleotide variantFabry disease
  • rs398123227Conflicting interpretationssingle nucleotide variantFabry disease
  • rs727505292Conflicting interpretationssingle nucleotide variantFabry disease|Migalastat response
  • rs730880441Conflicting interpretationssingle nucleotide variantFabry disease
  • rs797044613Conflicting interpretationssingle nucleotide variantFabry disease
  • rs869312345Conflicting interpretationssingle nucleotide variantFabry disease
  • rs138886989Likely benignsingle nucleotide variantCardiovascular phenotype|Fabry disease
  • rs1057516429Likely pathogenicsingle nucleotide variantFabry disease
  • rs28935196Likely pathogenicsingle nucleotide variantFabry disease
  • rs372966991Likely pathogenicsingle nucleotide variant
  • rs398123199Likely pathogenicsingle nucleotide variant
  • rs398123205Likely pathogenicsingle nucleotide variant
  • rs398123222Likely pathogenicsingle nucleotide variant
  • rs869312134Likely pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312135Likely pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312142Likely pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312148Likely pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312150Likely pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312151Likely pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312153Likely pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312165Likely pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312246Likely pathogenicsingle nucleotide variant
  • rs886044879Likely pathogenicsingle nucleotide variantFabry disease
  • rs886044906Likely pathogenicsingle nucleotide variant
  • rs104894827Pathogenicsingle nucleotide variantFabry disease
  • rs104894829Pathogenicsingle nucleotide variantFabry disease
  • rs104894830Pathogenicsingle nucleotide variantFabry disease, cardiac variant|Fabry disease
  • rs104894831Pathogenicsingle nucleotide variantFabry disease
  • rs104894832Pathogenicsingle nucleotide variantFabry disease
  • rs104894834Pathogenicsingle nucleotide variantFabry disease
  • rs104894835Pathogenicsingle nucleotide variantFabry disease
  • rs104894836Pathogenicsingle nucleotide variantFabry disease
  • rs104894837Pathogenicsingle nucleotide variantFabry disease
  • rs104894838Pathogenicsingle nucleotide variantFabry disease
  • rs104894839Pathogenicsingle nucleotide variantFabry disease
  • rs104894840Pathogenicsingle nucleotide variantFabry disease
  • rs104894841Pathogenicsingle nucleotide variantFabry disease
  • rs104894842Pathogenicsingle nucleotide variantFabry disease
  • rs104894843Pathogenicsingle nucleotide variantFabry disease
  • rs104894844Pathogenicsingle nucleotide variantFabry disease
  • rs104894846Pathogenicsingle nucleotide variantFabry disease, cardiac variant
  • rs104894847Pathogenicsingle nucleotide variantFabry disease, cardiac variant
  • rs104894848Pathogenicsingle nucleotide variantFabry disease
  • rs104894849Pathogenicsingle nucleotide variantFabry disease
  • rs104894851Pathogenicsingle nucleotide variantFabry disease
  • rs104894852Pathogenicsingle nucleotide variantFabry disease
  • rs1057519609PathogenicDeletionFabry disease
  • rs1057521047Pathogenicsingle nucleotide variantFabry disease
  • rs1060500747Pathogenicsingle nucleotide variantFabry disease
  • rs1064796601PathogenicMicrosatelliteFabry disease
  • rs112341092Pathogenicsingle nucleotide variantFabry disease
  • rs113173389Pathogenicsingle nucleotide variantFabry disease
  • rs140329381Pathogenicsingle nucleotide variant
  • rs28935195Pathogenicsingle nucleotide variantFabry disease
  • rs28935197Pathogenicsingle nucleotide variantFabry disease|Cardiovascular phenotype|Hypertrophic cardiomyopathy|Fabry disease|Cardiomyopathy
  • rs28935485Pathogenicsingle nucleotide variantFabry disease, cardiac variant
  • rs28935486Pathogenicsingle nucleotide variantFabry disease
  • rs28935487Pathogenicsingle nucleotide variantFabry disease
  • rs28935488Pathogenicsingle nucleotide variantFabry disease
  • rs28935489Pathogenicsingle nucleotide variantFabry disease
  • rs28935491Pathogenicsingle nucleotide variantFabry disease
  • rs28935492Pathogenicsingle nucleotide variantFabry disease
  • rs28935493Pathogenicsingle nucleotide variantFabry disease
  • rs28935494Pathogenicsingle nucleotide variantFabry disease
  • rs28935495Pathogenicsingle nucleotide variantFabry disease
  • rs397515870Pathogenicsingle nucleotide variantFabry disease|Cardiomyopathy
  • rs398123197PathogenicInsertionFabry disease
  • rs398123198PathogenicMicrosatelliteFabry disease
  • rs398123201Pathogenicsingle nucleotide variantFabry disease
  • rs398123207Pathogenicsingle nucleotide variant
  • rs398123210Pathogenicsingle nucleotide variant
  • rs398123211Pathogenicsingle nucleotide variant
  • rs398123212Pathogenicsingle nucleotide variant
  • rs398123216Pathogenicsingle nucleotide variant
  • rs398123217Pathogenicsingle nucleotide variantFabry disease
  • rs398123219Pathogenicsingle nucleotide variant
  • rs398123220Pathogenicsingle nucleotide variantFabry disease
  • rs398123221Pathogenicsingle nucleotide variantFabry disease
  • rs398123224Pathogenicsingle nucleotide variantFabry disease
  • rs398123225PathogenicMicrosatelliteFabry disease
  • rs398123226Pathogenicsingle nucleotide variantFabry disease
  • rs398123228Pathogenicsingle nucleotide variantFabry disease
  • rs398123229PathogenicDeletionFabry disease
  • rs727503072Pathogenicsingle nucleotide variantFabry disease
  • rs727503948Pathogenicsingle nucleotide variant
  • rs727503949Pathogenicsingle nucleotide variantFabry disease
  • rs727504348Pathogenicsingle nucleotide variantFabry disease|Hypertrophic cardiomyopathy|Fabry disease
  • rs730880444Pathogenicsingle nucleotide variant
  • rs730880447Pathogenicsingle nucleotide variant
  • rs730880451Pathogenicsingle nucleotide variantFabry disease
  • rs730880453PathogenicDeletionFabry disease
  • rs730880454PathogenicDeletionFabry disease
  • rs797044499Pathogenicsingle nucleotide variant
  • rs797044500PathogenicDeletionFabry disease
  • rs797044669Pathogenicsingle nucleotide variantFabry disease
  • rs797044670PathogenicMicrosatellite
  • rs797044727Pathogenicsingle nucleotide variant
  • rs797044746Pathogenicsingle nucleotide variant
  • rs797044747Pathogenicsingle nucleotide variantFabry disease
  • rs797044748Pathogenicsingle nucleotide variantFabry disease
  • rs797044768Pathogenicsingle nucleotide variant
  • rs797044774Pathogenicsingle nucleotide variantFabry disease
  • rs797044775Pathogenicsingle nucleotide variantFabry disease
  • rs797044776Pathogenicsingle nucleotide variantFabry disease
  • rs869312136Pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312137Pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312138Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312139Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312140Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312141Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312145Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312146Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312149Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312154Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312158Pathogenicsingle nucleotide variantMigalastat response|Fabry disease
  • rs869312160Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312163Pathogenicsingle nucleotide variantFabry disease|Migalastat response
  • rs869312227Pathogenicsingle nucleotide variantFabry disease
  • rs869312344Pathogenicsingle nucleotide variantFabry disease
  • rs878853698Pathogenicsingle nucleotide variantFabry disease
  • rs879253955PathogenicDeletionFabry disease
  • rs879253990PathogenicDeletion
  • rs879254022Pathogenicsingle nucleotide variantFabry disease
  • rs886039136PathogenicDuplicationCardiovascular phenotype|Fabry disease
  • rs886041315Pathogenicsingle nucleotide variantFabry disease
  • rs886044766Pathogenicsingle nucleotide variantFabry disease
  • rs886044829PathogenicDeletionFabry disease
  • rs886044843Pathogenicsingle nucleotide variantFabry disease
  • rs886044845Pathogenicsingle nucleotide variant
  • rs886044860Pathogenicsingle nucleotide variantFabry disease
  • rs886044900Pathogenicsingle nucleotide variant
  • rs397515873Uncertain significancesingle nucleotide variant
  • rs397515874Uncertain significancesingle nucleotide variant
  • rs398123202Uncertain significancesingle nucleotide variant
  • rs398123204Uncertain significancesingle nucleotide variant
  • rs781838005Uncertain significancesingle nucleotide variantMigalastat response|Fabry disease
  • rs782449839Uncertain significancesingle nucleotide variantMigalastat response|Fabry disease|Hypertrophic cardiomyopathy 1|Stroke
  • rs782598150Uncertain significancesingle nucleotide variant
  • rs869312164Uncertain significancesingle nucleotide variantMigalastat response|Fabry disease

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.