ClinVar Miner

Submissions for variant NM_015915.5(ATL1):c.630+9G>A

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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 RCV002741995 SCV003022353 likely benign Hereditary spastic paraplegia 3A 2023-07-03 criteria provided, single submitter clinical testing

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