ClinVar Miner

Submissions for variant NM_139319.3(SLC17A8):c.*1521dup

dbSNP: rs59689031
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
Illumina Laboratory Services, Illumina RCV000344089 SCV000375143 uncertain significance Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693076 SCV005191940 uncertain significance not provided criteria provided, single submitter not provided

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