ClinVar Miner

List of variants studied for Fanconi anemia complementation group D2 by OMIM

Included ClinVar conditions (1):
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Total variants: 5
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HGVS dbSNP
FANCD2, 376A-G
FANCD2, EX17 DEL
NM_033084.5(FANCD2):c.3707G>A (p.Arg1236His) rs121917786
NM_033084.5(FANCD2):c.904C>T (p.Arg302Trp) rs121917787
NM_033084.5(FANCD2):c.958C>T (p.Gln320Ter) rs121917788

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