ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.5304G>A (p.Glu1768=) (rs41303346)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000039590 SCV000063279 benign not specified 2012-04-17 criteria provided, single submitter clinical testing Glu1768Glu in exon 24 of GPR98: This variant is not expected to have clinical si gnificance because it does not alter an amino acid residue, is not located withi n the splice consensus sequence, and has been identified in 2% (133/6694) of Eur opean American chromosomes and 0.5% (16/3782) of African American chromosomes in a broad population by the NHLBI Exome sequencing project (http://evs.gs.washing ton.edu/EVS/; dbSNP rs41303346).
GeneDx RCV000039590 SCV000168701 benign not specified 2013-04-12 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Athena Diagnostics Inc RCV000710451 SCV000840672 benign not provided 2017-10-05 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000039590 SCV001158945 benign not specified 2018-07-31 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV001155224 SCV001316641 likely benign Usher syndrome, type 2C 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 and internal cut-off values, a variant classified as likely benign is not then subjected to further curation. The score for this variant resulted in a classification of likely benign for this disease.
Genetic Services Laboratory, University of Chicago RCV000039590 SCV000193269 likely benign not specified no assertion criteria provided clinical testing

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