ClinVar Miner

List of variants reported as uncertain significance for familial visceral amyloidosis by Johns Hopkins Genomics, Johns Hopkins University

Included ClinVar conditions (6):

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

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.1615G>A (p.Glu539Lys)	rs1190260696	0.00001
NM_021871.4(FGA):c.1760C>G (p.Thr587Arg)	rs1309799184	0.00001

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