ClinVar Miner

List of variants in gene FGG reported as uncertain significance for Familial dysfibrinogenemia

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_021870.3(FGG):c.571G>A (p.Gly191Arg)	rs6063	0.00339
NM_021870.3(FGG):c.709T>C (p.Tyr237His)	rs762488338	0.00005

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