List of variants reported as likely pathogenic for thrombophilia due to protein C deficiency, autosomal recessive

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000312.4(PROC):c.703A>C (p.Lys235Gln)	rs370086431	0.00015
NM_000312.4(PROC):c.541T>G (p.Phe181Val)	rs199469470	0.00005
NM_000312.4(PROC):c.752C>T (p.Ala251Val)	rs568121876	0.00003
NM_000312.4(PROC):c.169C>T (p.Arg57Trp)	rs757583846	0.00002
NM_000312.4(PROC):c.124C>T (p.Arg42Cys)	rs774572099	0.00001
NM_000312.4(PROC):c.631C>T (p.Arg211Trp)	rs121918143	0.00001
NM_000312.4(PROC):c.303C>A (p.Cys101Ter)	rs764808999

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