List of variants in gene F8 reported as uncertain significance by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000132.4(F8):c.1724A>C (p.Lys575Thr)	rs2073367952
NM_000132.4(F8):c.1969T>C (p.Tyr657His)	rs2124082280
NM_000132.4(F8):c.2573C>T (p.Pro858Leu)	rs2124053040
NM_000132.4(F8):c.2776C>T (p.Pro926Ser)	rs2124052509
NM_000132.4(F8):c.3144G>T (p.Trp1048Cys)	rs1060499784
NM_000132.4(F8):c.3744A>T (p.Leu1248Phe)	rs2124050282
NM_000132.4(F8):c.5005A>G (p.Ile1669Val)	rs2124047405
NM_000132.4(F8):c.5267A>T (p.Glu1756Val)	rs2124000688
NM_000132.4(F8):c.5815G>C (p.Ala1939Pro)	rs1603432979
NM_000132.4(F8):c.5863C>G (p.Gln1955Glu)	rs2123996340
NM_000132.4(F8):c.6123G>C (p.Gln2041His)	rs2123993594
NM_000132.4(F8):c.6322G>C (p.Ala2108Pro)	rs2148583727
NM_000132.4(F8):c.6709G>T (p.Ala2237Ser)	rs2148567205
NM_000132.4(F8):c.6834G>T (p.Glu2278Asp)	rs2072682134

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