Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

MEGF10

multiple EGF like domains 10

Chromosome
5
Cytoband
5q23.2
Variants (rsID)
68

MEGF10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q23.2). Its official name is “multiple EGF like domains 10”. The reference table lists 68 variants (rsID) for this gene.

Clinically classified variants

16 reference-table entries with clinical significance.

  • rs17164935Benignsingle nucleotide variantMEGF10-Related Myopathy
  • rs35591368Benignsingle nucleotide variantMEGF10-Related Myopathy
  • rs3756721Benignsingle nucleotide variantMEGF10-Related Myopathy
  • rs3812055Benignsingle nucleotide variantMEGF10-Related Myopathy
  • rs79904777Benignsingle nucleotide variantMEGF10-Related Myopathy
  • rs113794264Conflicting interpretationssingle nucleotide variantMEGF10-Related Myopathy
  • rs116500162Conflicting interpretationssingle nucleotide variantMEGF10-Related Myopathy
  • rs140563851Conflicting interpretationssingle nucleotide variantMEGF10-Related Myopathy
  • rs142947482Conflicting interpretationssingle nucleotide variantMEGF10-Related Myopathy
  • rs185480820Conflicting interpretationssingle nucleotide variantMEGF10-Related Myopathy
  • rs73783802Conflicting interpretationssingle nucleotide variantMEGF10-Related Myopathy
  • rs78847357Conflicting interpretationssingle nucleotide variantMEGF10-Related Myopathy
  • rs147731088Likely benignsingle nucleotide variantMEGF10-Related Myopathy
  • rs387907071Pathogenicsingle nucleotide variantMEGF10-Related Myopathy
  • rs41298304Uncertain significancesingle nucleotide variantMEGF10-Related Myopathy
  • rs78069165Uncertain significancesingle nucleotide variantMEGF10-Related Myopathy

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.