List of variants in gene CDHR1 reported as benign for perceptual disorders

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_033100.4(CDHR1):c.2439T>C (p.Thr813=)	rs3814213	0.58250
NM_033100.4(CDHR1):c.*2798G>A	rs10509491	0.56109
NM_033100.4(CDHR1):c.477A>G (p.Ala159=)	rs4933975	0.52743
NM_001171971.3(CDHR1):c.2145G>A (p.Leu715=)	rs4244947	0.49096
NM_033100.4(CDHR1):c.1662A>G (p.Glu554=)	rs10749482	0.42520
NM_033100.4(CDHR1):c.*3768G>C	rs2279229	0.36843
NM_033100.4(CDHR1):c.*3020G>A	rs11594855	0.17242
NM_033100.4(CDHR1):c.*3504A>C	rs114617516	0.01276
NM_033100.4(CDHR1):c.*1360C>A	rs73317918	0.00938
NM_033100.4(CDHR1):c.*767C>T	rs60075421	0.00937
NM_033100.4(CDHR1):c.2473C>A (p.Pro825Thr)	rs201515900

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.