ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.23295A>C (p.Glu7765Asp)

gnomAD frequency: 0.00003  dbSNP: rs774259283
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
Eurofins Ntd Llc (ga) RCV000278636 SCV000338702 uncertain significance not provided 2016-09-25 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002282105 SCV002571016 uncertain significance not specified 2022-07-18 criteria provided, single submitter clinical testing

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