ClinVar Miner

Submissions for variant NM_000441.2(SLC26A4):c.2089+9A>G

gnomAD frequency: 0.00016  dbSNP: rs369504960
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
Invitae RCV000978844 SCV001126778 likely benign not provided 2024-01-16 criteria provided, single submitter clinical testing
Natera, Inc. RCV001278044 SCV001465036 uncertain significance Pendred syndrome 2020-08-13 no assertion criteria provided clinical testing

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