ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.105G>A (p.Thr35=)

gnomAD frequency: 0.00021  dbSNP: rs144566508
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698201 SCV000526506 likely benign not provided 2020-11-10 criteria provided, single submitter clinical testing
Invitae RCV000897597 SCV001041751 likely benign Intellectual disability, autosomal dominant 8 2024-01-21 criteria provided, single submitter clinical testing

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