ClinVar Miner

Submissions for variant NM_000036.3(AMPD1):c.1974+16G>T

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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 RCV002667557 SCV002983247 likely benign Muscle AMP deaminase deficiency 2022-11-15 criteria provided, single submitter clinical testing

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