ClinVar Miner

List of variants reported as uncertain significance for Thrombophilia due to thrombin defect by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000506.3(F2):c.598G>A (p.Glu200Lys)	rs62623459	0.00138
NM_000506.5(F2):c.371G>A (p.Arg124Gln)	rs139148365	0.00022

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