ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.*1C>T

gnomAD frequency: 0.00048  dbSNP: rs148811960
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001719960 SCV000513441 likely benign not provided 2019-01-03 criteria provided, single submitter clinical testing
Ambry Genetics RCV000620003 SCV000737316 uncertain significance Cardiovascular phenotype 2017-10-10 criteria provided, single submitter clinical testing There is insufficient or conflicting evidence for classification of this alteration.
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV000769184 SCV000900560 uncertain significance Cardiomyopathy 2016-05-05 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000154731 SCV000204411 not provided not specified 2013-04-26 no assertion provided clinical testing

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