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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.