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

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000129.4(F13A1):c.980G>A (p.Arg327Gln)	rs121913072	0.00002
NM_021871.4(FGA):c.117del (p.Val40fs)	rs762964798

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