ClinVar Miner

Submissions for variant NM_001182.5(ALDH7A1):c.1318-7C>T

dbSNP: rs1554098186
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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 RCV003631614 SCV004404963 likely benign Pyridoxine-dependent epilepsy 2023-05-31 criteria provided, single submitter clinical testing

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