ClinVar Miner

Submissions for variant NM_002334.4(LRP4):c.3536+22C>A

dbSNP: rs964551
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001689520 SCV001915213 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730975 SCV001981450 benign Congenital myasthenic syndrome 17 2021-08-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730973 SCV001981451 benign Cenani-Lenz syndactyly syndrome 2021-08-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730974 SCV001981452 benign Sclerosteosis 2 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001689520 SCV005320238 benign not provided criteria provided, single submitter not provided

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