List of variants reported as likely pathogenic for coagulation protein disease by Institute of Human Genetics, University Hospital Muenster

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.1169T>C (p.Ile390Thr)	rs2124106062
NM_000132.4(F8):c.5306G>A (p.Gly1769Glu)
NM_000133.4(F9):c.391+5G>A	rs2148358021
NM_000552.5(VWF):c.4892G>A (p.Gly1631Asp)	rs2136411659

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