List of variants in gene CABP2 reported as likely pathogenic for Autosomal recessive nonsyndromic hearing loss 93

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: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_016366.3(CABP2):c.590T>C (p.Ile197Thr)	rs145369252	0.00068
NM_016366.3(CABP2):c.482del (p.Phe161fs)	rs368437370
NM_016366.3(CABP2):c.490-8C>A	rs776117741
NM_016366.3(CABP2):c.60C>A (p.Leu20=)

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.