ClinVar Miner

List of variants reported as likely pathogenic for Fanconi anemia complementation group D2 by Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota

Included ClinVar conditions (1):

Fanconi anemia complementation group D2

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.1278+6T>C	rs779894573	0.00001
NM_001018115.3(FANCD2):c.904C>T (p.Arg302Trp)	rs121917787	0.00001
NM_001018115.3(FANCD2):c.3095del (p.Asn1032fs)	rs1559399574

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