List of variants in gene CEP152 reported as benign by PreventionGenetics, part of Exact Sciences

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_001194998.2(CEP152):c.833-4G>A	rs58156069	0.39693
NM_001194998.2(CEP152):c.3466+8G>C	rs2306187	0.25704
NM_001194998.2(CEP152):c.2019-13G>A	rs9302144	0.05016
NM_001194998.2(CEP152):c.161C>T (p.Ser54Leu)	rs2289181	0.02268
NM_001194998.2(CEP152):c.1577+6G>A	rs78525896	0.01033
NM_001194998.2(CEP152):c.4857T>C (p.Asp1619=)	rs74986073	0.00651
NM_001194998.2(CEP152):c.1909-8G>C	rs116089174	0.00531
NM_001194998.2(CEP152):c.5115A>G (p.Pro1705=)	rs1048042	0.00273
NM_001194998.2(CEP152):c.4744T>C (p.Ser1582Pro)	rs77745570	0.00243
NM_001194998.2(CEP152):c.2681C>T (p.Ser894Phe)	rs145138194	0.00034
NM_001194998.2(CEP152):c.4757G>C (p.Arg1586Pro)	rs202237336	0.00029

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.