Gene entry
GCM2
GCM transcription factor 2
- Chromosome
- 6
- Cytoband
- 6p24.2
- Variants (rsID)
- 7
GCM2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p24.2). Its official name is “GCM transcription factor 2”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs104893959Pathogenicsingle nucleotide variantHypoparathyroidism, familial isolated, 2
- rs104893960Pathogenicsingle nucleotide variantHypoparathyroidism, familial isolated, 2
- rs142287570Uncertain significancesingle nucleotide variantFamilial hypoparathyroidism|Hyperparathyroidism 4
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.