ClinVar Miner

Submissions for variant NM_002291.3(LAMB1):c.4221C>T (p.Ser1407=)

gnomAD frequency: 0.00416  dbSNP: rs35082294
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000193108 SCV000247818 likely benign not specified 2015-07-20 criteria provided, single submitter clinical testing
GeneDx RCV000967063 SCV000526011 benign not provided 2019-01-04 criteria provided, single submitter clinical testing
Invitae RCV000967063 SCV001114433 benign not provided 2023-12-06 criteria provided, single submitter clinical testing

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