List of variants in gene CYP1B1 reported as likely benign 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000104.4(CYP1B1):c.-1-14C>T	rs4987134	0.02460
NM_000104.4(CYP1B1):c.*2371T>C	rs9309020	0.02296
NM_000104.4(CYP1B1):c.*926A>C	rs9341261	0.01416
NM_000104.4(CYP1B1):c.*2158T>C	rs112948057	0.01121
NM_000104.4(CYP1B1):c.*2261A>C	rs77534033	0.00985
NM_000104.4(CYP1B1):c.*1853G>T	rs9341265	0.00338

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