ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group B by Baylor Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.1317T>A (p.Ser439Arg)	rs776802337
NM_001018113.3(FANCB):c.2224T>C (p.Cys742Arg)	rs2092364017
NM_001018113.3(FANCB):c.83C>G (p.Ser28Cys)

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