ClinVar Miner

List of variants in gene AGBL1 reported as benign for Fuchs' endothelial dystrophy

Included ClinVar conditions (8):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001386094.1(AGBL1):c.1641G>T (p.Met547Ile)
NM_001386094.1(AGBL1):c.2423G>C (p.Ser808Thr)
NM_001386094.1(AGBL1):c.861C>T (p.Pro287=)

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