List of variants in gene CHRDL1 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_001143981.2(CHRDL1):c.207G>C (p.Glu69Asp)	rs2148509597
NM_001143981.2(CHRDL1):c.968G>T (p.Cys323Phe)	rs2148418567

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