ClinVar Miner

List of variants in gene combination F10, F7 reported as benign for congenital factor VII deficiency

Included ClinVar conditions (4):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.1172G>A (p.Arg391Gln)	rs6046	0.11103
NM_019616.4(F7):c.*770G>A	rs3093253	0.10963

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