Gene entry
MEGF8
multiple EGF like domains 8
- Chromosome
- 19
- Cytoband
- 19q13.2
- Variants (rsID)
- 9
MEGF8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.2). Its official name is “multiple EGF like domains 8”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs112167630Benignsingle nucleotide variantMEGF8-related Carpenter syndrome
- rs45623135Likely benignsingle nucleotide variantMEGF8-related Carpenter 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.
