ClinVar Miner

Submissions for variant NM_006059.4(LAMC3):c.521_522delinsAG (p.Pro174Gln)

dbSNP: rs386738954
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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 RCV000501706 SCV000595554 likely benign not specified 2015-09-30 criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000501706 SCV000709168 benign not specified 2017-06-14 criteria provided, single submitter clinical testing
Invitae RCV002056856 SCV002436054 benign not provided 2024-02-01 criteria provided, single submitter clinical testing

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