ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.306C>T (p.Asp102=) (rs200850130)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000710140 SCV000527650 likely benign not provided 2021-02-01 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000710140 SCV000613548 benign not provided 2017-10-25 criteria provided, single submitter clinical testing
Invitae RCV000550789 SCV000638240 likely benign Epilepsy, focal, with speech disorder and with or without mental retardation 2017-05-17 criteria provided, single submitter clinical testing

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