ClinVar Miner

Submissions for variant NM_000228.3(LAMB3):c.822+33G>C

dbSNP: rs2072940
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000247734 SCV000303084 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537715 SCV001754659 benign Amelogenesis imperfecta type 1A 2021-07-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537744 SCV001754692 benign Junctional epidermolysis bullosa gravis of Herlitz 2021-07-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537745 SCV001754693 benign Junctional epidermolysis bullosa, non-Herlitz type 2021-07-08 criteria provided, single submitter clinical testing
GeneDx RCV001651117 SCV001866253 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001651117 SCV005286861 benign not provided criteria provided, single submitter not provided

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