ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.45975G>C (p.Val15325=)

dbSNP: rs2154211097
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
Clinical Genetics, Academic Medical Center RCV001699710 SCV001920561 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001699710 SCV001955215 benign not specified no assertion criteria provided clinical testing

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