List of variants in gene TCF4 reported as benign for corneal disorder

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_001083962.2(TCF4):c.789+23C>T	rs1788027	0.53241
NM_001083962.2(TCF4):c.1941A>G (p.Ser647=)	rs8766	0.37317
NM_001083962.2(TCF4):c.305-165C>T	rs17522826	0.15868

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