ADAMTS13 rs387906345: what the research says
This variant is a pathogenic deletion associated with Upshaw-Schulman syndrome, a rare form of thrombotic thrombocytopenic purpura.
Rare
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This variant is associated with Upshaw-Schulman syndrome, a rare hereditary form of thrombotic thrombocytopenic purpura.
This pathogenic variant is linked to Upshaw-Schulman syndrome, which can cause severe complications during pregnancy.
Variants in this gene are linked to protein activity levels that may impact dermal microvasculature and skin health.
A rare variant linked to specific phenotypic expressions in facial structure and connective tissue appearance.