ClinVar Miner

List of variants reported as pathogenic for Fuchs' endothelial dystrophy by Molecular Genetics Lab, CHRU Brest

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_001083962.2(TCF4):c.1733G>A (p.Arg578His)	rs121909123
NM_001083962.2(TCF4):c.306_307del (p.Ser102fs)
NM_001083962.2(TCF4):c.710_711insT (p.Tyr238fs)

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