ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group J by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_032043.3(BRIP1):c.1255C>T (p.Arg419Trp) rs150624408 0.00026

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