ClinVar Miner

List of variants reported as likely pathogenic for Deep venous thrombosis; Thromboembolism by NIHR Bioresource Rare Diseases, University of Cambridge

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000312.4(PROC):c.125G>A (p.Arg42His)	rs369504169	0.00001
NM_000312.4(PROC):c.352T>C (p.Phe118Leu)	rs1553424043

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