List of variants in gene F9 reported as likely pathogenic 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.224G>A (p.Arg75Gln)	rs137852228	0.00001
NM_000133.4(F9):c.1214A>T (p.Asp405Val)
NM_000133.4(F9):c.1229A>T (p.Asp410Val)	rs1928125452
NM_000133.4(F9):c.1289G>A (p.Ser430Asn)	rs1569333062
NM_000133.4(F9):c.1328T>C (p.Ile443Thr)	rs137852268
NM_000133.4(F9):c.161A>T (p.Glu54Val)	rs1569481966
NM_000133.4(F9):c.205T>A (p.Cys69Ser)	rs2148356172
NM_000133.4(F9):c.235G>A (p.Glu79Lys)	rs1927499978
NM_000133.4(F9):c.478G>C (p.Gly160Arg)	rs1927768022
NM_000133.4(F9):c.786T>G (p.Ile262Met)	rs2148367254

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