ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group O by Mendelics

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.784T>G (p.Leu262Val) rs149331537 0.00014
NM_058216.3(RAD51C):c.-2C>T rs876658796 0.00001
NM_058216.3(RAD51C):c.3G>A (p.Met1Ile) rs769053886 0.00001
NM_058216.3(RAD51C):c.16T>G (p.Phe6Val) rs749498443
NM_058216.3(RAD51C):c.912T>G (p.Ser304Arg) rs876659009

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