ClinVar Miner

Submissions for variant NM_000441.2(SLC26A4):c.1438-7dup

dbSNP: rs753586849
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000671630 SCV000796622 uncertain significance Pendred syndrome 2017-12-20 criteria provided, single submitter clinical testing
GeneDx RCV002225713 SCV002504218 likely benign not provided 2020-11-17 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Invitae RCV002225713 SCV004295496 benign not provided 2023-02-14 criteria provided, single submitter clinical testing

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