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Gene entry

ADAMTS2

ADAM metallopeptidase with thrombospondin type 1 motif 2

Chromosome
5
Cytoband
5q35.3
Variants (rsID)
112

ADAMTS2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q35.3). Its official name is “ADAM metallopeptidase with thrombospondin type 1 motif 2”. The reference table lists 112 variants (rsID) for this gene.

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Clinically classified variants

11 reference-table entries with clinical significance.

  • rs149391669Benignsingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type
  • rs1863918Benignsingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type
  • rs2271211Benignsingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type|Ehlers-Danlos syndrome
  • rs35445112Benignsingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type|Ehlers-Danlos syndrome
  • rs61757478Benignsingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type|Ehlers-Danlos syndrome
  • rs66565583Benignsingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type
  • rs112155474Conflicting interpretationssingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type|Ehlers-Danlos syndrome
  • rs143764421Conflicting interpretationssingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type|Ehlers-Danlos syndrome
  • rs200806292Conflicting interpretationssingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type|Ehlers-Danlos syndrome
  • rs137853147Likely pathogenicsingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type
  • rs137853146Pathogenicsingle nucleotide variantEhlers-Danlos syndrome, dermatosparaxis type

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.