List of variants in gene combination CYP4V2, KLKB1 reported as benign for corneal disorder

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_207352.4(CYP4V2):c.*1781A>C	rs6842047	0.89083
NM_207352.4(CYP4V2):c.*725C>T	rs10033577	0.89040
NM_207352.4(CYP4V2):c.*741C>T	rs10033581	0.81342
NM_207352.4(CYP4V2):c.*1236A>T	rs1053094	0.45426
NM_207352.4(CYP4V2):c.*2399C>T	rs56413992	0.15680
NM_207352.4(CYP4V2):c.*1148A>G	rs10011736	0.07494
NM_207352.4(CYP4V2):c.*364T>G	rs7697077

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