ClinVar Miner

Submissions for variant NM_002334.4(LRP4):c.4006C>T (p.Pro1336Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005046808 SCV005683173 uncertain significance Cenani-Lenz syndactyly syndrome; Sclerosteosis 2; Congenital myasthenic syndrome 17 2024-04-04 criteria provided, single submitter clinical testing

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