List of variants reported as uncertain significance for inherited thrombophilia by Revvity Omics, Revvity

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000361.3(THBD):c.1406A>G (p.Asp469Gly)	rs373741115	0.00005
NM_000361.3(THBD):c.965G>A (p.Arg322Gln)	rs146549103
NM_000488.4(SERPINC1):c.269T>G (p.Phe90Cys)	rs2526594931

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