List of variants in gene CYP1B1 reported as benign for Glaucoma 3A

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000104.4(CYP1B1):c.*695G>T	rs10916	0.76280
NM_000104.4(CYP1B1):c.*350C>A	rs162562	0.67224
NM_000104.4(CYP1B1):c.*975A>G	rs2855658	0.48745
NM_000104.4(CYP1B1):c.142C>G (p.Arg48Gly)	rs10012	0.36324
NM_000104.4(CYP1B1):c.355G>T (p.Ala119Ser)	rs1056827	0.35167
NM_000104.4(CYP1B1):c.-1-12C>T	rs2617266	0.28114
NM_000104.4(CYP1B1):c.*2409A>T	rs162549	0.18874
NM_000104.4(CYP1B1):c.729G>C (p.Val243=)	rs9341249	0.06879
NM_000104.4(CYP1B1):c.*1871C>T	rs9341266	0.03671
NM_000104.4(CYP1B1):c.564C>A (p.Gly188=)	rs9341247	0.02411
NM_000104.4(CYP1B1):c.1103G>A (p.Arg368His)	rs79204362	0.00125

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.