ClinVar Miner

Submissions for variant NM_014946.3(SPAST):c.832G>A (p.Val278Met) (rs369908571)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000518464 SCV000615398 uncertain significance not provided 2017-12-19 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000764403 SCV000895460 uncertain significance Spastic paraplegia 4, autosomal dominant 2018-10-31 criteria provided, single submitter clinical testing

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