ClinVar Miner

List of variants reported as benign for thrombophilia due to protein C deficiency, autosomal recessive by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (2):

Thrombophilia due to protein C deficiency, autosomal recessive
Thrombophilia due to protein C deficiency, autosomal recessive; Thrombophilia due to protein C deficiency, autosomal dominant

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000312.4(PROC):c.1107G>A (p.Pro369=)	rs61731660	0.01266
NM_000312.4(PROC):c.400+13G>A	rs116738363	0.01228

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