ClinVar Miner

Submissions for variant NM_000228.3(LAMB3):c.1289-186G>A

dbSNP: rs61822212
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001537709 SCV001754653 benign Amelogenesis imperfecta type 1A 2021-07-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537710 SCV001754654 benign Junctional epidermolysis bullosa gravis of Herlitz 2021-07-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537711 SCV001754655 benign Junctional epidermolysis bullosa, non-Herlitz type 2021-07-08 criteria provided, single submitter clinical testing
GeneDx RCV001709727 SCV001938462 benign not provided 2018-11-12 criteria provided, single submitter clinical testing

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