ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.10972C>T (p.Arg3658Trp) (rs115155117)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000248252 SCV000312144 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000868348 SCV001009663 likely benign Spastic paraplegia 2020-11-23 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV001288374 SCV001475439 likely benign not provided 2020-06-26 criteria provided, single submitter clinical testing

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