List of variants in gene F7 reported as likely 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)
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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_019616.4(F7):c.64+983G>A	rs3093238	0.01072
NM_019616.4(F7):c.64+8C>T	rs10482844	0.00989
NM_019616.4(F7):c.1104C>T (p.Ala368=)	rs6044	0.00216
NM_019616.4(F7):c.64+4C>T	rs187128791	0.00178
NM_019616.4(F7):c.*1503C>T	rs551279029	0.00007
NM_019616.4(F7):c.1292C>T (p.Ser431Leu)	rs1490539322
NM_019616.4(F7):c.84A>C (p.Glu28Asp)	rs2142212240

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