ClinVar Miner

Submissions for variant NM_014112.5(TRPS1):c.-393_-392dup

dbSNP: rs759303878
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 RCV000381705 SCV000471512 uncertain significance Trichorhinophalangeal syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004696053 SCV005196093 uncertain significance not provided criteria provided, single submitter not provided

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