ClinVar Miner

Submissions for variant NM_001287174.2(ABCC8):c.2823+17A>G (rs2106865)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000144989 SCV000303801 benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000576868 SCV000677120 benign not provided 2017-04-12 criteria provided, single submitter clinical testing
Invitae RCV000576868 SCV001729170 benign not provided 2020-12-08 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000144989 SCV000192025 likely benign not specified no assertion criteria provided clinical testing

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