ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.35876-2A>G

dbSNP: rs1577134819
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000997495 SCV001152958 likely pathogenic not provided 2019-05-01 criteria provided, single submitter clinical testing

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