ClinVar Miner

List of variants reported as uncertain significance for Fuchs' endothelial dystrophy by Mendelics

Included ClinVar conditions (8):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001174096.2(ZEB1):c.2522A>C (p.Gln841Pro)	rs118020901	0.00680
NM_001386094.1(AGBL1):c.3157C>T (p.Arg1053Trp)	rs185919705	0.00200
NM_152336.4(AGBL1):c.3323+1G>A	rs79072327

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