ClinVar Miner

List of variants reported as likely benign for Fanconi anemia complementation group B by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.2477C>T (p.Thr826Met)	rs201436396	0.00032
NM_001018113.3(FANCB):c.1105-26TATT[7]	rs398123537

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