ClinVar Miner

Submissions for variant NM_000441.2(SLC26A4):c.*1875G>C (rs886061892)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000342301 SCV000466153 uncertain significance Nonsyndromic Hearing Loss, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000401884 SCV000466154 uncertain significance Pendred syndrome 2016-06-14 criteria provided, single submitter clinical testing

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