List of variants in gene FANCB reported as likely benign by Genetic Services Laboratory, University of Chicago

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

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001018113.3(FANCB):c.262G>A (p.Gly88Arg)	rs142101123	0.00058
NM_001018113.3(FANCB):c.989T>C (p.Ile330Thr)	rs200161949	0.00047
NM_001018113.3(FANCB):c.2090C>T (p.Pro697Leu)	rs147255018	0.00037
NM_001018113.3(FANCB):c.2452A>G (p.Arg818Gly)	rs143131218	0.00036
NM_001018113.3(FANCB):c.2394C>T (p.Val798=)	rs190579053	0.00005
NM_001018113.3(FANCB):c.2265A>G (p.Leu755=)	rs777812135	0.00001
NM_001018113.3(FANCB):c.1105-26TATT[7]	rs398123537
NM_001018113.3(FANCB):c.1317T>C (p.Ser439=)	rs776802337
NM_001018113.3(FANCB):c.2109A>G (p.Thr703=)	rs1555904303

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