ClinVar Miner

Submissions for variant NM_005562.3(LAMC2):c.405-31T>C

gnomAD frequency: 0.25565  dbSNP: rs10911285
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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 RCV001537730 SCV001754678 benign Junctional epidermolysis bullosa gravis of Herlitz 2021-07-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537731 SCV001754679 benign Junctional epidermolysis bullosa, non-Herlitz type 2021-07-08 criteria provided, single submitter clinical testing
GeneDx RCV001676036 SCV001893009 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001676036 SCV005284752 benign not provided criteria provided, single submitter not provided

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