ClinVar Miner

Submissions for variant NM_021956.5(GRIK2):c.724-7del

dbSNP: rs2243352
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
Genetic Services Laboratory, University of Chicago RCV000194476 SCV000247514 benign not specified 2014-05-08 criteria provided, single submitter clinical testing
GeneDx RCV001770145 SCV002004202 likely benign not provided 2019-11-11 criteria provided, single submitter clinical testing

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