ClinVar Miner

Submissions for variant NM_031418.4(ANO3):c.1447+57AC[21]

dbSNP: rs71047866
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001616274 SCV001839104 benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260227 SCV002539161 benign Dystonia 24 2021-12-05 criteria provided, single submitter clinical testing

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