List of variants in gene F7 reported as benign for 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.64+9G>A	rs6039	0.15932
NM_019616.4(F7):c.459C>T (p.His153=)	rs6042	0.12147
NM_019616.4(F7):c.219G>A (p.Glu73=)	rs36208758	0.01020
NM_019616.4(F7):c.*620C>T	rs151109093	0.00308
NM_019616.4(F7):c.483C>T (p.Asp161=)	rs6040	0.00046
NM_019616.4(F7):c.64+941C>T	rs189409610	0.00006

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