ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.51437-1G>C

dbSNP: rs2055916646
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
CeGaT Center for Human Genetics Tuebingen RCV001090563 SCV001246174 pathogenic not provided 2020-06-01 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001090563 SCV003822838 uncertain significance not provided 2019-07-02 criteria provided, single submitter clinical testing

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