ClinVar Miner

Submissions for variant NM_016464.5(TMEM138):c.128+19T>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003071736 SCV003459019 likely benign Joubert syndrome 16 2022-10-13 criteria provided, single submitter clinical testing

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