ClinVar Miner

Submissions for variant NM_001182.5(ALDH7A1):c.696-16G>T

dbSNP: rs2480304878
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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 RCV003631740 SCV004492110 likely benign Pyridoxine-dependent epilepsy 2022-12-06 criteria provided, single submitter clinical testing

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