ClinVar Miner

Submissions for variant NM_006420.3(ARFGEF2):c.2406G>A (p.Arg802=)

gnomAD frequency: 0.00001  dbSNP: rs756651881
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000501012 SCV000593298 uncertain significance not specified 2016-03-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060101 SCV002445673 likely benign not provided 2021-12-02 criteria provided, single submitter clinical testing

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