ClinVar Miner

List of variants in gene F11 reported as likely benign for Hereditary factor XI deficiency disease

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Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_000128.4(F11):c.1717-48A>G rs5966 0.06916
NM_000128.4(F11):c.-54G>A rs4253814 0.01170
NM_000128.4(F11):c.1016G>T (p.Cys339Phe) rs5967 0.00586
NM_000128.4(F11):c.1304+12G>A rs116667976 0.00295
NM_000128.4(F11):c.453C>T (p.Tyr151=) rs34807019 0.00248
NM_000128.4(F11):c.*884C>T rs117035365 0.00024
NM_000128.4(F11):c.1843G>A (p.Val615Met) rs202061241 0.00016
NM_000128.4(F11):c.1683C>T (p.Ala561=) rs770473069 0.00003
NM_000128.4(F11):c.1304+25_1304+28del rs778294619
NM_000128.4(F11):c.1481-34G>T rs2289253
NM_000128.4(F11):c.1576+51C>A rs2289254

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