Gene entry
AGK
acylglycerol kinase
- Chromosome
- 7
- Cytoband
- 7q34
- Variants (rsID)
- 17
AGK is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q34). Its official name is “acylglycerol kinase”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs113085050Benignsingle nucleotide variantSengers syndrome|Cataract 38|Sengers syndrome|Cataract 38
- rs41275003Conflicting interpretationssingle nucleotide variantCataract 38|Sengers syndrome|Cataract 38|Sengers syndrome
- rs763068104Conflicting interpretationssingle nucleotide variantSengers syndrome|Cataract 38
- rs35269563Likely benignsingle nucleotide variantSengers syndrome|Cataract 38
- rs387907025Pathogenicsingle nucleotide variantSengers syndrome
- rs766413410Pathogenicsingle nucleotide variantCataract 38|Sengers syndrome|Inborn genetic diseases|Autosomal recessive AGK-related phenotype
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.