ClinVar Miner

List of variants in gene combination ADAMTS13, LOC130002909 reported as likely benign for congenital thrombotic thrombocytopenic purpura

Included ClinVar conditions (1):

Upshaw-Schulman syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_139025.4(ADAMTS13):c.-357T>C	rs34265876	0.07895

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