ClinVar Miner

List of variants in gene SLC17A8 reported as likely pathogenic for autosomal dominant nonsyndromic hearing loss 25

Included ClinVar conditions (1):

Autosomal dominant nonsyndromic hearing loss 25

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: 2

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_139319.3(SLC17A8):c.634C>A (p.Pro212Thr)	rs1952754017
NM_139319.3(SLC17A8):c.903+1_903+6del

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.