ClinVar Miner

List of variants reported as uncertain significance for Plasminogen deficiency, type I by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000301.5(PLG):c.112A>G (p.Lys38Glu)	rs73015965	0.00282
NM_000301.5(PLG):c.86A>C (p.Gln29Pro)	rs1051644668	0.00001

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