ClinVar Miner

Submissions for variant NM_006757.4(TNNT3):c.83-48A>G

gnomAD frequency: 0.80906  dbSNP: rs629990
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253853 SCV000311581 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001544251 SCV001763251 benign Arthrogryposis, distal, type 2B2 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001696197 SCV001916180 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001696197 SCV005321255 benign not provided criteria provided, single submitter not provided

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