ClinVar Miner

Submissions for variant NM_001134831.2(AHI1):c.2623+18T>A

dbSNP: rs2128009104
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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 RCV002158153 SCV002425900 likely benign Familial aplasia of the vermis 2024-03-11 criteria provided, single submitter clinical testing

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