List of variants reported as likely pathogenic for hematologic disorder by CSER _CC_NCGL, University of Washington

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000312.4(PROC):c.125G>A (p.Arg42His)	rs369504169	0.00001
NM_000312.4(PROC):c.631C>T (p.Arg211Trp)	rs121918143	0.00001
NM_000313.4(PROS1):c.728-1G>A	rs368074804

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