List of variants in gene FANCB reported as likely pathogenic for Fanconi anemia complementation group B

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.1570C>T (p.Gln524Ter)
NM_001018113.3(FANCB):c.781C>T (p.Arg261Ter)	rs2147445599
NM_001018113.3(FANCB):c.972del (p.Lys324fs)

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