ClinVar Miner

Submissions for variant NM_031418.4(ANO3):c.1290-13G>T

dbSNP: rs56325113
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001707882 SCV001936563 benign not provided 2018-09-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073316 SCV002385759 benign Dystonic disorder 2025-02-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002260373 SCV002539155 benign Dystonia 24 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001707882 SCV005317882 benign not provided criteria provided, single submitter not provided

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