ClinVar Miner

List of variants studied for Myocardial infarction, susceptibility to; Congenital factor VII deficiency

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Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_019616.4(F7):c.64+4C>T rs187128791 0.00178
NM_019616.4(F7):c.1025G>A (p.Arg342Gln) rs121964926 0.00118
NM_019616.4(F7):c.1267G>A (p.Glu423Lys) rs3093248 0.00113
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.364+1G>A rs1056071555 0.00006
NM_019616.4(F7):c.845C>T (p.Ala282Val) rs121964931 0.00006
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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