ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.64481C>T (p.Pro21494Leu)

gnomAD frequency: 0.00001  dbSNP: rs587780492
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
Genetic Services Laboratory, University of Chicago RCV000118774 SCV000153323 uncertain significance not provided 2014-01-24 criteria provided, single submitter clinical testing

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