List of variants reported as pathogenic for blood coagulation disease by New York Genome Center

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.2561G>A (p.Arg854Gln)	rs41276738	0.00377
NM_000132.4(F8):c.6532C>T (p.Arg2178Cys)	rs137852464

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