ClinVar Miner

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

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Total variants: 18
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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+11C>G rs1263551026 0.00001
NM_058216.3(RAD51C):c.145+13G>A rs1177750681 0.00001
NM_058216.3(RAD51C):c.145+10C>A
NM_058216.3(RAD51C):c.145+10C>G
NM_058216.3(RAD51C):c.145+10C>T
NM_058216.3(RAD51C):c.145+11C>T
NM_058216.3(RAD51C):c.145+12T>C
NM_058216.3(RAD51C):c.145+13G>C rs1177750681
NM_058216.3(RAD51C):c.145+14A>G rs1567783355
NM_058216.3(RAD51C):c.145+15T>C rs780116924
NM_058216.3(RAD51C):c.145+16G>A rs1471520258
NM_058216.3(RAD51C):c.145+17G>A rs369854656
NM_058216.3(RAD51C):c.145+17G>T rs369854656
NM_058216.3(RAD51C):c.145+18C>A
NM_058216.3(RAD51C):c.145+19A>G
NM_058216.3(RAD51C):c.145+7_145+17del rs2143681500
NM_058216.3(RAD51C):c.145+8C>T rs1555592121

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