ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group B by Leiden Open Variation Database

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.2027T>C (p.Leu676Pro)	rs1601977531
NM_001018113.3(FANCB):c.2059G>T (p.Glu687Ter)	rs1601977510
NM_152633.4(FANCB):c.-70-3463_951dup

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