Variants from ClinGen Coagulation Factor Deficiency Variant Curation Expert Panel, Clingen

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:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
44	20	10	0	18	92

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
F8	27	9	5	8	49
F9	17	11	5	10	43

Condition and significance breakdown #

Total conditions: 2

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Condition	pathogenic	likely pathogenic	uncertain significance	benign	total
Hereditary factor VIII deficiency disease	27	9	5	8	49
Hereditary factor IX deficiency disease	17	11	5	10	43

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