ClinVar Miner

Submissions for variant NM_005562.3(LAMC2):c.641-80C>T

gnomAD frequency: 0.25699  dbSNP: rs2296307
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001537734 SCV001754682 benign Junctional epidermolysis bullosa gravis of Herlitz 2021-07-08 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537735 SCV001754683 benign Junctional epidermolysis bullosa, non-Herlitz type 2021-07-08 criteria provided, single submitter clinical testing
GeneDx RCV001655829 SCV001869400 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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