ClinVar Miner

Submissions for variant NM_001038603.3(MARVELD2):c.30G>A (p.Arg10=)

gnomAD frequency: 0.00023  dbSNP: rs143592561
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000175654 SCV000227184 uncertain significance not provided 2015-03-20 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000337147 SCV000458115 uncertain significance Autosomal recessive nonsyndromic hearing loss 49 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
Invitae RCV000175654 SCV001066027 likely benign not provided 2023-02-18 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV001195336 SCV001365682 likely benign not specified 2012-04-30 criteria provided, single submitter clinical testing Arg10Arg in Exon 02 of MARVELD2: This variant is not expected to have clinical significance because it does not alter an amino acid residue, is not located within the splice consensus sequence, and has been identified in 3/7020 European American chromosomes from a broad population by the NHLBI Exome Sequencing Project (http://evs.gs.washington.edu/EVS; dbSNP rs143592561).

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