ClinVar Miner

Submissions for variant NM_001042472.3(ABHD12):c.788-10_788-7del (rs565270893)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000180549 SCV000233013 uncertain significance not provided 2015-05-20 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000180549 SCV001142898 likely benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Invitae RCV000180549 SCV001729499 benign not provided 2020-11-20 criteria provided, single submitter clinical testing

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