ClinVar Miner

Submissions for variant NM_000365.6(TPI1):c.*541dup

dbSNP: rs201871949
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 RCV000327220 SCV000381022 uncertain significance Triosephosphate isomerase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693130 SCV005191663 uncertain significance not provided criteria provided, single submitter not provided

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