ClinVar Miner

Submissions for variant NM_014363.6(SACS):c.21-162C>G

dbSNP: rs578105700
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001590778 SCV001826868 likely benign not provided 2019-01-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506698 SCV002805521 likely benign Charlevoix-Saguenay spastic ataxia 2021-10-08 criteria provided, single submitter clinical testing

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