ClinVar Miner

Submissions for variant NM_001330677.2(TBX15):c.519C>T (p.Tyr173=)

gnomAD frequency: 0.01515  dbSNP: rs61730013
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000965561 SCV001112831 benign not provided 2025-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000965561 SCV001936334 benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003338883 SCV004049026 benign Pelviscapular dysplasia 2023-04-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000965561 SCV005281055 benign not provided criteria provided, single submitter not provided

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