List of variants in gene F7 reported as likely pathogenic for Myocardial infarction, susceptibility to; Congenital factor VII deficiency

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.995C>T (p.Ala332Val)	rs36209567	0.00038
NM_019616.4(F7):c.413A>G (p.Gln138Arg)	rs200016360	0.00008
NM_019616.4(F7):c.1325del (p.Pro442fs)	rs750457207
NM_019616.4(F7):c.64G>A (p.Val22Ile)
NM_019616.4(F7):c.739+3_739+6del	rs754785708
NM_019616.4(F7):c.80del (p.Glu27fs)

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