ClinVar Miner

Submissions for variant NC_000011.10:g.77156886G>A

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000825983 SCV000967471 uncertain significance not specified 2018-03-07 criteria provided, single submitter clinical testing The p.Arg206His variant in MYO7A has been reported in 4 Asian individuals with h earing loss. Three of them did not have another MYO7A variant reported, while th e fourth carried two additional MYO7A variants and the individual's mother with normal hearing also carried the p.Arg206His variant (Hu 2004, Su 2009, Nishio 20 17). This variant has been identified in 0.16% (31/18868) of East Asian chromoso mes by the Genome Aggregation Database (gnomAD, http://gnomad.broadinstitute.org ; dbSNP rs781998354). Although this variant has been seen in the general populat ion, its frequency is not high enough to rule out a pathogenic role. Computation al prediction tools and conservation analyses suggest that this variant may impa ct the protein, though this information is not predictive enough to determine pa thogenicity. In summary, the clinical significance of the p.Arg206His variant is uncertain. ACMG/AMP Criteria applied: PP3.

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.