ClinVar Miner

Submissions for variant NM_006757.4(TNNT3):c.32-149A>T

gnomAD frequency: 0.76033  dbSNP: rs2734500
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001544250 SCV001763250 benign Arthrogryposis, distal, type 2B2 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV000024565 SCV001843135 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Leiden Muscular Dystrophy (TNNT3) RCV000024565 SCV000045869 not provided not provided 2012-03-18 no assertion provided curation

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