ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.91325A>C (p.Lys30442Thr)

gnomAD frequency: 0.00006  dbSNP: rs370086155
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 RCV000993505 SCV001146529 uncertain significance not provided 2018-09-26 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000993505 SCV003822961 uncertain significance not provided 2019-09-25 criteria provided, single submitter clinical testing

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