ClinVar Miner

Submissions for variant NM_001510.4(GRID2):c.101A>G (p.Asp34Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003751616 SCV004562248 uncertain significance Autosomal recessive spinocerebellar ataxia 18 2023-11-22 criteria provided, single submitter clinical testing

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