List of variants in gene FGB reported as likely benign for congenital afibrinogenemia

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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_005141.5(FGB):c.1113A>G (p.Ser371=)	rs6057	0.00574
NM_005141.5(FGB):c.794C>T (p.Pro265Leu)	rs6054	0.00275
NM_005141.5(FGB):c.682A>G (p.Thr228Ala)	rs149599496	0.00272
NM_005141.5(FGB):c.534G>C (p.Lys178Asn)	rs201909029	0.00038
NM_005141.5(FGB):c.510T>A (p.Asn170Lys)	rs149963684	0.00011

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