ClinVar Miner

Submissions for variant NM_015046.7(SETX):c.2981A>G (p.Asp994Gly) (rs149546633)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001089117 SCV001016302 likely benign Amyotrophic lateral sclerosis type 4; Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000874168 SCV001145542 benign not provided 2019-04-29 criteria provided, single submitter clinical testing

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