ClinVar Miner

Submissions for variant NM_006757.3(TNNT3):c.367-9T>C (rs76471485)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000331506 SCV000369767 likely benign Arthrogryposis multiplex congenita 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000388403 SCV000369768 likely benign Arthrogryposis multiplex congenita distal 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000246488 SCV000311574 benign not specified 2016-02-15 criteria provided, single submitter clinical testing

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