ClinVar Miner

List of variants in gene combination FANCD2, LOC107303338 reported as likely pathogenic for Fanconi anemia complementation group D2

Included ClinVar conditions (1):
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Total variants: 2
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NM_033084.5(FANCD2):c.2094_2096CCT[1] (p.Leu700del) rs869312805
NM_033084.5(FANCD2):c.904C>T (p.Arg302Trp) rs121917787

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