List of variants in gene FGB reported as pathogenic by OMIM

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005141.5(FGB):c.139C>T (p.Arg47Ter)	rs121909625	0.00003
NM_005141.5(FGB):c.1148T>G (p.Leu383Arg)	rs121909621
NM_005141.5(FGB):c.1244+1G>T	rs606231224
NM_005141.5(FGB):c.1289G>A (p.Gly430Asp)	rs121909622
NM_005141.5(FGB):c.605T>A (p.Leu202Gln)	rs121909624
NM_005141.5(FGB):c.958+13C>T	rs606231223

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