ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.96526T>A (p.Tyr32176Asn)

gnomAD frequency: 0.00006  dbSNP: rs377291343
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 RCV000517268 SCV000616190 uncertain significance not specified 2016-10-28 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003139731 SCV003824771 uncertain significance not provided 2019-07-08 criteria provided, single submitter clinical testing

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