Variants in gene F5 with conflicting interpretations "pathogenic" and "benign"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_000130.5(F5):c.1601= (p.Arg534=)	rs6025	0.98238
NM_000130.4(F5):c.1601G>A (p.Arg534Gln)	rs6025	0.01762

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