List of variants in gene combination CYP4V2, KLKB1 reported as likely 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_207352.4(CYP4V2):c.*1638G>A	rs72646300	0.07687
NM_207352.4(CYP4V2):c.*2106G>T	rs72646302	0.01061
NM_207352.4(CYP4V2):c.*2303G>C	rs576134216	0.00006

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