Gene entry
GPD1L
glycerol-3-phosphate dehydrogenase 1 like
- Chromosome
- 3
- Cytoband
- 3p22.3
- Variants (rsID)
- 12
GPD1L is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p22.3). Its official name is “glycerol-3-phosphate dehydrogenase 1 like”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs72546642Benignsingle nucleotide variantBrugada syndrome|Cardiovascular phenotype
- rs112122950Conflicting interpretationssingle nucleotide variantSudden cardiac death|Brugada syndrome
- rs72552292Uncertain significancesingle nucleotide variantBrugada syndrome 2|Cardiovascular phenotype|Brugada syndrome
- rs72552294Uncertain significancesingle nucleotide variantBrugada syndrome 2|Cardiovascular phenotype|Brugada syndrome
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.