List of variants reported as likely pathogenic for Congenital prothrombin deficiency by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000506.5(F2):c.1070A>G (p.Glu357Gly)	rs2134533215
NM_000506.5(F2):c.118C>T (p.Arg40Trp)
NM_000506.5(F2):c.1270G>A (p.Val424Met)	rs1310397756
NM_000506.5(F2):c.1496G>A (p.Gly499Glu)	rs2134537035
NM_000506.5(F2):c.995G>C (p.Gly332Ala)	rs2134532862

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