Variants in gene F8 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.1018G>A (p.Glu340Lys)	rs781954986	0.00019
NM_000132.4(F8):c.396A>C (p.Glu132Asp)	rs137852388	0.00018
NM_000132.4(F8):c.3169G>A (p.Glu1057Lys)	rs28933673	0.00014
NM_000132.4(F8):c.1094A>G (p.Tyr365Cys)	rs375241473	0.00007
NM_000132.4(F8):c.5954G>A (p.Arg1985Gln)	rs1490417405	0.00001
NM_000132.4(F8):c.6623A>G (p.Gln2208Arg)	rs782198570	0.00001
NM_000132.4(F8):c.2009TCT[2] (p.Phe672del)	rs1476178386
NM_000132.4(F8):c.2150G>T (p.Arg717Leu)	rs942909873
NM_000132.4(F8):c.766T>A (p.Tyr256Asn)	rs1569559955

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