Gene entry
ADAMTS13
ADAM metallopeptidase with thrombospondin type 1 motif 13
- Chromosome
- 9
- Cytoband
- 9q34.2
- Variants (rsID)
- 24
ADAMTS13 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q34.2). Its official name is “ADAM metallopeptidase with thrombospondin type 1 motif 13”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs28503257Benignsingle nucleotide variantUpshaw-Schulman syndrome
- rs28647808Benignsingle nucleotide variantUpshaw-Schulman syndrome
- rs34024143Benignsingle nucleotide variantUpshaw-Schulman syndrome
- rs11575933Conflicting interpretationssingle nucleotide variantUpshaw-Schulman syndrome
- rs142572218Conflicting interpretationssingle nucleotide variantUpshaw-Schulman syndrome
- rs147112200Conflicting interpretationssingle nucleotide variantUpshaw-Schulman syndrome
- rs148312697Conflicting interpretationssingle nucleotide variantUpshaw-Schulman syndrome
- rs121908470Pathogenicsingle nucleotide variantUpshaw-Schulman syndrome
- rs121908472Pathogenicsingle nucleotide variantUpshaw-Schulman syndrome
- rs121908473Pathogenicsingle nucleotide variantUpshaw-Schulman 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.