ClinVar Miner

List of variants in gene combination LOC129390903, RAD51C reported as likely pathogenic for Fanconi anemia complementation group O

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.705+1G>T rs876658644
NM_058216.3(RAD51C):c.705G>T (p.Lys235Asn) rs755849719

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