ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.11581-3dup

dbSNP: rs34894132
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000039512 SCV000063201 benign not specified 2012-03-08 criteria provided, single submitter clinical testing 11581-3_11581-2insC in intron 55 of GPR98: This variant is not expected to have clinical significance because it has been found frequently in the general popula tion (rs34894132 - 7 entries) and in 9/13 cases from our laboratory.
PreventionGenetics, part of Exact Sciences RCV000039512 SCV000314849 benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000039512 SCV000331602 benign not specified 2015-11-22 criteria provided, single submitter clinical testing
GeneDx RCV001516999 SCV000730779 benign not provided 2018-05-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001516999 SCV001725383 benign not provided 2025-02-03 criteria provided, single submitter clinical testing

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