Gene entry
ADAMTS17
ADAM metallopeptidase with thrombospondin type 1 motif 17
- Chromosome
- 15
- Cytoband
- 15q26.3
- Variants (rsID)
- 167
ADAMTS17 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q26.3). Its official name is “ADAM metallopeptidase with thrombospondin type 1 motif 17”. The reference table lists 167 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs117381111Benignsingle nucleotide variantWeill-Marchesani 4 syndrome, recessive
- rs2573625Benignsingle nucleotide variantWeill-Marchesani 4 syndrome, recessive
- rs2573652Benignsingle nucleotide variantWeill-Marchesani 4 syndrome, recessive
- rs2581341Benignsingle nucleotide variantWeill-Marchesani 4 syndrome, recessive
- rs28567966Benignsingle nucleotide variantWeill-Marchesani 4 syndrome, recessive
- rs200327256Uncertain significancesingle nucleotide variantWeill-Marchesani 4 syndrome, recessive
- rs200371613Uncertain significancesingle nucleotide variantWeill-Marchesani 4 syndrome, recessive
- rs201644342Uncertain significancesingle nucleotide variant
Other listed variants
- rs728879
- rs748432
- rs892898
- rs892902
- rs892905
- rs934596
- rs958983
- rs999486
- rs1383547
- rs1480958
- rs1561046
- rs1975453
- rs1994009
- rs2035342
- rs2086455
- rs2170282
- rs2199932
- rs2418489
- rs2440465
- rs2573679
- rs2622530
- rs2727110
- rs2727122
- rs2727182
- rs2727184
- rs2900634
- rs2900636
- rs3891624
- rs4297665
- rs4516211
- rs4533267
- rs4602021
- rs4641722
- rs4965278
- rs4965284
- rs4965293
- rs4965294
- rs4965567
- rs4965573
- rs4965587
- rs4965593
- rs4965623
- rs5026360
- rs6598301
- rs6598308
- rs6598321
- rs6598324
- rs7164647
- rs7173620
- rs7180014
- rs7180604
- rs7182059
- rs7182422
- rs7495703
- rs7497860
- rs8024362
- rs8024746
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.