ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.6469G>A (p.Val2157Met)

gnomAD frequency: 0.00001  dbSNP: rs144723817
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001038542 SCV001202017 likely benign not provided 2023-11-22 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001155318 SCV001316740 uncertain significance Usher syndrome type 2C 2017-07-05 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). Publications were found based on this search. However, the evidence from the literature, in combination with allele frequency data from public databases where available, was not sufficient to rule this variant in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.

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