ClinVar Miner

Submissions for variant NM_006757.4(TNNT3):c.68-14C>T

gnomAD frequency: 0.00084  dbSNP: rs202175253
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000306102 SCV000369761 uncertain significance Arthrogryposis multiplex congenita distal 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000353956 SCV000369762 uncertain significance Arthrogryposis multiplex congenita 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002056186 SCV002342425 benign not provided 2024-01-25 criteria provided, single submitter clinical testing

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