ClinVar Miner

List of variants studied for Fanconi anemia complementation group U by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.643C>T (p.Arg215Ter) rs143153871 0.00006
NM_005431.2(XRCC2):c.272G>A (p.Arg91Gln) rs776959023 0.00002

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