List of variants reported as likely pathogenic for blood coagulation disease by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.995C>T (p.Ala332Val)	rs36209567	0.00038
NM_000212.3(ITGB3):c.1699C>T (p.Gln567Ter)	rs1057518837
NM_000212.3(ITGB3):c.749A>G (p.Asp250Gly)	rs1057518838
NM_019616.4(F7):c.1325del (p.Pro442fs)	rs750457207

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