ClinVar Miner

Submissions for variant NM_144612.6(LOXHD1):c.5328G>A (p.Glu1776=) (rs749182319)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000725135 SCV000334356 uncertain significance not provided 2015-09-14 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000392596 SCV000731923 uncertain significance not specified 2017-11-22 criteria provided, single submitter clinical testing Variant classified as Uncertain Significance - Favor Benign. The p.Glu1776Glu v ariant in LOXHD1 has not been previously reported in individuals with hearing lo ss, but has been identified in 5/24794 Latino chromosomes by the Genome Aggregat ion Database (gnomAD,; dbSNP rs749182319). Alth ough this variant has been seen in the general population, its frequency is not high enough to rule out a pathogenic role. It has also been reported in ClinVar (Variation ID: 282748). The variant does not alter an amino acid residue and is not located within the splice consensus sequence; however, this information is n ot sufficient to rule out an impact to splicing or expression of the gene. In su mmary, while the clinical significance of the p.Glu1776Glu variant is uncertain, these data suggest that it is more likely to be benign. ACMG/AMP Criteria appli ed: PM2, BP7.

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