ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.32096-5T>G

gnomAD frequency: 0.00001  dbSNP: rs551230637
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000714014 SCV000844677 uncertain significance not provided 2018-06-27 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000714014 SCV004033823 uncertain significance not provided 2023-07-01 criteria provided, single submitter clinical testing TTN: PM2, BP4

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