List of variants in gene MCFD2 reported as uncertain significance for Factor V and factor VIII, combined deficiency of, type 1

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_139279.6(MCFD2):c.*1289T>C	rs527427772	0.00002
NM_139279.6(MCFD2):c.2780_2781del	rs886056109
NM_139279.6(MCFD2):c.3072_3073insGG	rs559484016

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