ClinVar Miner

Submissions for variant NM_001348323.3(TRIP12):c.1133+21del

dbSNP: rs11373804
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001638362 SCV001849955 benign not provided 2021-05-17 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838715 SCV002098791 benign Clark-Baraitser syndrome 2021-09-10 criteria provided, single submitter clinical testing

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