ClinVar Miner

Submissions for variant NM_000426.4(LAMA2):c.4909G>C (p.Glu1637Gln)

dbSNP: rs138303386
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000992262 SCV001144407 uncertain significance not provided 2019-01-23 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001819700 SCV002065142 uncertain significance not specified 2017-09-25 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000992262 SCV003808129 uncertain significance not provided 2019-07-11 criteria provided, single submitter clinical testing

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