ClinVar Miner

Submissions for variant NM_002291.3(LAMB1):c.1945G>A (p.Asp649Asn)

gnomAD frequency: 0.00147  dbSNP: rs142386151
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 RCV000500852 SCV000595525 uncertain significance not specified 2016-12-01 criteria provided, single submitter clinical testing
Invitae RCV000895013 SCV001039030 likely benign not provided 2023-10-20 criteria provided, single submitter clinical testing
GeneDx RCV000895013 SCV001776372 likely benign not provided 2019-10-07 criteria provided, single submitter clinical testing

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