ClinVar Miner

Submissions for variant NM_014946.4(SPAST):c.1834G>A (p.Gly612Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002289477 SCV002581122 uncertain significance Hereditary spastic paraplegia 4 2022-07-25 criteria provided, single submitter clinical testing

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