List of variants reported as likely pathogenic for hematologic disorder by Clingen Thrombosis Variant Curation Expert Panel, ClinGen

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000488.4(SERPINC1):c.439A>G (p.Thr147Ala)	rs2227606	0.00184
NM_000488.4(SERPINC1):c.449A>C (p.Gln150Pro)	rs765445413	0.00001
NM_000488.4(SERPINC1):c.1274G>C (p.Arg425Pro)	rs121909549
NM_000488.4(SERPINC1):c.1306G>A (p.Ala436Thr)	rs121909546
NM_000488.4(SERPINC1):c.1316C>T (p.Pro439Leu)	rs121909555
NM_000488.4(SERPINC1):c.235C>A (p.Arg79Ser)	rs121909547
NM_000488.4(SERPINC1):c.624+1G>A	rs1572090079

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