ClinVar Miner

Submissions for variant NM_002291.3(LAMB1):c.3481C>T (p.Arg1161Cys)

gnomAD frequency: 0.00014  dbSNP: rs146018013
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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 RCV000504123 SCV000595521 uncertain significance not specified 2016-02-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000998893 SCV001155226 uncertain significance not provided 2019-01-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000998893 SCV002483978 benign not provided 2023-11-14 criteria provided, single submitter clinical testing

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