ClinVar Miner

Submissions for variant NM_144612.6(LOXHD1):c.4376-6G>A (rs369463541)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000150969 SCV000198645 uncertain significance not specified 2015-05-22 criteria provided, single submitter clinical testing Variant classified as Uncertain Significance - Favor Benign. The c.4376-6G>A var iant in LOXHD1 has been previously identified by our laboratory in 1 individual with hearing loss who carried a homozygous variant in another gene that was suff icient to explain their disease. It has also been identified in 1/8398 European chromosomes by the Exome Aggregation Consortium (ExAC, http://exac.broadinstitut; dbSNP rs369463541). This variant is located in the 3' splice region. Comp utational tools do not suggest an impact to splicing. In addition, the guanine ( G) nucleotide at position c.4376-6 is not conserved in mammals or evolutionarily distant species and 9 mammals carry an adenine (A), supporting that a change at this position may be tolerated. However, this information is not predictive eno ugh to rule out pathogenicity. In summary, while the clinical significance of th e c.4376-6G>A variant is uncertain, the presence of the variant nucleotide in ot her species and predicted lack of impact on splicing suggest that it is more lik ely to be benign.
Illumina Clinical Services Laboratory,Illumina RCV000367009 SCV000408724 uncertain significance Nonsyndromic Hearing Loss, Recessive 2016-06-14 criteria provided, single submitter clinical testing

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