List of variants in gene FANCB reported as likely benign for Fanconi anemia complementation group B; VACTERL association, X-linked, with or without hydrocephalus

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.1067C>T (p.Ser356Leu)	rs142304943	0.00046
NM_001018113.3(FANCB):c.1393T>C (p.Ser465Pro)	rs143976596	0.00038
NM_001018113.3(FANCB):c.1995C>T (p.Pro665=)	rs192743430	0.00024
NM_001018113.3(FANCB):c.504C>G (p.Ser168=)	rs373738816	0.00010
NM_001018113.3(FANCB):c.330A>C (p.Leu110=)	rs201633684	0.00008
NM_001018113.3(FANCB):c.1494G>T (p.Lys498Asn)	rs199510538	0.00005
NM_001018113.3(FANCB):c.2385T>C (p.Ser795=)	rs1034395123	0.00002
NM_001018113.3(FANCB):c.1105-26TATT[4]	rs398123537
NM_001018113.3(FANCB):c.1767A>G (p.Thr589=)	rs964099207
NM_001018113.3(FANCB):c.706G>A (p.Val236Met)	rs746389250

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