ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.17843T>C (p.Ile5948Thr)

gnomAD frequency: 0.00001  dbSNP: rs772946744
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity Omics RCV003137102 SCV003818359 uncertain significance not provided 2020-02-21 criteria provided, single submitter clinical testing

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