List of variants in gene F9 reported as uncertain significance for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000133.4(F9):c.1196T>C (p.Phe399Ser)	rs2148368081
NM_000133.4(F9):c.196G>A (p.Glu66Lys)	rs1569481975
NM_000133.4(F9):c.262T>C (p.Trp88Arg)
NM_000133.4(F9):c.413A>G (p.Asn138Ser)	rs2148361153
NM_000133.4(F9):c.517G>A (p.Ala173Thr)	rs865782271
NM_000133.4(F9):c.637A>T (p.Asn213Tyr)	rs1057524310
NM_000133.4(F9):c.800A>C (p.His267Pro)	rs1447015296
NM_000133.4(F9):c.87A>G (p.Thr29=)	rs2148353000
NM_000133.4(F9):c.934T>G (p.Tyr312Asp)	rs1569332828
NM_000133.4(F9):c.980T>C (p.Leu327Pro)

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