ClinVar Miner

Submissions for variant NM_002334.4(LRP4):c.3700-21C>G

dbSNP: rs2306032
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001694494 SCV001908053 benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730962 SCV001981447 benign Congenital myasthenic syndrome 17 2021-08-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730960 SCV001981448 benign Cenani-Lenz syndactyly syndrome 2021-08-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001730961 SCV001981449 benign Sclerosteosis 2 2021-08-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001694494 SCV005320236 benign not provided criteria provided, single submitter not provided

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