ClinVar Miner

Submissions for variant NM_001044385.3(TMEM237):c.1159+16A>C

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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 RCV005110890 SCV005728967 likely benign Joubert syndrome 14 2024-11-12 criteria provided, single submitter clinical testing

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