ClinVar Miner

Submissions for variant NM_015915.5(ATL1):c.1374A>G (p.Thr458=)

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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 RCV003107228 SCV003782814 likely benign Hereditary spastic paraplegia 3A 2023-04-05 criteria provided, single submitter clinical testing

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