ClinVar Miner

List of variants reported as pathogenic for Fanconi anemia complementation group R

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_002875.5(RAD51):c.391A>C (p.Thr131Pro) rs1895530875
NM_002875.5(RAD51):c.877G>A (p.Ala293Thr) rs1057519413

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