ClinVar Miner

Submissions for variant NM_001182.5(ALDH7A1):c.99C>T (p.Leu33=)

dbSNP: rs1418934195
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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 RCV001404244 SCV001606141 likely benign Pyridoxine-dependent epilepsy 2018-08-12 criteria provided, single submitter clinical testing

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