List of variants in gene combination CYP1B1, LOC128772254 reported as uncertain significance for corneal disorder

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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_000104.4(CYP1B1):c.1319T>G (p.Phe440Cys)	rs771737035	0.00007
NM_000104.4(CYP1B1):c.1406G>A (p.Arg469Gln)	rs747324108	0.00001
NM_000104.4(CYP1B1):c.1345G>T (p.Asp449Tyr)	rs149049138

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