List of variants in gene combination LOC130059718, ZNF469 reported as uncertain significance 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001367624.2(ZNF469):c.3183C>T (p.Arg1061=)	rs756703220	0.00001
NM_001367624.2(ZNF469):c.3255G>C (p.Glu1085Asp)	rs886052401

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