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

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.402A>G (p.Leu134=)	rs147260208	0.00701
NM_001018113.3(FANCB):c.2342A>G (p.Glu781Gly)	rs140363445	0.00010
NM_001018113.3(FANCB):c.-232G>A	rs756766337	0.00009
NM_001018113.3(FANCB):c.1817G>A (p.Ser606Asn)	rs148560784	0.00009
NM_001018113.3(FANCB):c.1216C>T (p.Arg406Trp)	rs1364046604

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