ClinVar Miner

List of variants reported as likely benign for Fanconi anemia, complementation group U by Mendelics

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Total variants: 3

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HGVS	dbSNP
NM_005431.2(XRCC2):c.39+8C>G	rs200363289
NM_005431.2(XRCC2):c.40-16T>C	rs41274991
NM_005431.2(XRCC2):c.808T>G (p.Phe270Val)	rs145085742

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