ClinVar Miner

Submissions for variant NM_001348323.3(TRIP12):c.2625_2629del (p.Asn876fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003148446 SCV003836232 likely pathogenic Clark-Baraitser syndrome 2022-01-24 criteria provided, single submitter clinical testing

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