ClinVar Miner

Submissions for variant NM_002334.4(LRP4):c.860G>C (p.Trp287Ser)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005051452 SCV005684018 uncertain significance Cenani-Lenz syndactyly syndrome; Sclerosteosis 2; Congenital myasthenic syndrome 17 2024-06-04 criteria provided, single submitter clinical testing
Center for Computational Biology & Bioinformatics, University of California, San Diego RCV004574917 SCV005050051 uncertain significance Meniere disease 2024-06-03 no assertion criteria provided research

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