List of variants in gene combination LOC106014249, PAX6 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001368894.2(PAX6):c.-368G>A	rs886048206	0.00006
NM_001368894.2(PAX6):c.-430G>C	rs886048207	0.00002
NM_001368894.2(PAX6):c.-501del	rs886048208
NM_001368894.2(PAX6):c.-507T>C	rs886048209

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