ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.428-14_428-8del

dbSNP: rs370823033
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000970605 SCV001118194 benign not provided 2017-06-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002489406 SCV002799190 likely benign Donnai-Barrow syndrome 2021-09-28 criteria provided, single submitter clinical testing

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