ClinVar Miner

Submissions for variant NM_012188.5(FOXI1):c.965_967del (p.Phe322del)

dbSNP: rs886060400
Minimum review status: Collection method:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000349533 SCV000456203 uncertain significance Pendred syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000395183 SCV000456204 uncertain significance Nonsyndromic Hearing Loss, Mixed 2016-06-14 criteria provided, single submitter clinical testing

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