ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.52397A>G (p.Asp17466Gly)

gnomAD frequency: 0.00001  dbSNP: rs377156953
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
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001806752 SCV002051118 uncertain significance not specified 2021-12-14 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003136164 SCV003826646 uncertain significance not provided 2022-09-20 criteria provided, single submitter clinical testing

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