ClinVar Miner

Submissions for variant NM_002291.3(LAMB1):c.3594C>T (p.His1198=)

gnomAD frequency: 0.00081  dbSNP: rs566055806
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
GeneDx RCV001550542 SCV001770881 likely benign not provided 2021-06-21 criteria provided, single submitter clinical testing
Invitae RCV001550542 SCV003467794 benign not provided 2023-12-22 criteria provided, single submitter clinical testing

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