ClinVar Miner

List of variants in gene combination LOC130061310, RAD51C reported as uncertain significance for Fanconi anemia complementation group O

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Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.145+12T>G rs377297129 0.00024
NM_058216.3(RAD51C):c.145+5C>A rs876660577 0.00001
NM_058216.3(RAD51C):c.145+5C>T rs876660577 0.00001
NM_058216.3(RAD51C):c.145+18C>T rs763292447
NM_058216.3(RAD51C):c.145+2_145+3insTT rs1567783294
NM_058216.3(RAD51C):c.145+3A>G rs536596205
NM_058216.3(RAD51C):c.145+4A>G rs1598449822

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