List of variants in gene combination LOC129929400, UBIAD1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_013319.3(UBIAD1):c.-311C>T	rs886045057	0.00006
NM_013319.2(UBIAD1):c.-337C>T	rs547031506
NM_013319.3(UBIAD1):c.-310C>T	rs1471509365

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