Gene entry
AGRN
agrin
- Chromosome
- 1
- Cytoband
- 1p36.33
- Variants (rsID)
- 24
AGRN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.33). Its official name is “agrin”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
16 reference-table entries with clinical significance.
- rs111818381Benignsingle nucleotide variantCongenital myasthenic syndrome 8
- rs113288277Benignsingle nucleotide variantCongenital myasthenic syndrome 8
- rs138288952Benignsingle nucleotide variantCongenital myasthenic syndrome 8
- rs2275811Benignsingle nucleotide variant
- rs2799064Benignsingle nucleotide variant
- rs79016973Benignsingle nucleotide variantCongenital myasthenic syndrome 8
- rs143324306Conflicting interpretationssingle nucleotide variantCongenital myasthenic syndrome 8
- rs144164397Conflicting interpretationssingle nucleotide variantCongenital myasthenic syndrome 8
- rs144245019Conflicting interpretationssingle nucleotide variantCongenital myasthenic syndrome 8
- rs145444272Conflicting interpretationssingle nucleotide variantCongenital myasthenic syndrome 8
- rs146243145Conflicting interpretationssingle nucleotide variantCongenital myasthenic syndrome 8
- rs536657086Conflicting interpretationssingle nucleotide variantCongenital myasthenic syndrome 8
- rs544749044Conflicting interpretationssingle nucleotide variantCongenital myasthenic syndrome 8
- rs142620337Likely benignsingle nucleotide variantCongenital myasthenic syndrome 8
- rs149268246Uncertain significancesingle nucleotide variantCongenital myasthenic syndrome 8
- rs149762107Uncertain significancesingle nucleotide variantCongenital myasthenic syndrome 8
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.