ClinVar Miner

Submissions for variant NM_018834.6(MATR3):c.358A>G (p.Arg120Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003132603 SCV003808302 uncertain significance Amyotrophic lateral sclerosis type 21 2019-05-30 criteria provided, single submitter clinical testing

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