ClinVar Miner

Submissions for variant NM_198999.3(SLC26A5):c.971+179_971+180del

dbSNP: rs141013688
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001610048 SCV001840952 benign not provided 2018-12-17 criteria provided, single submitter clinical testing

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