ClinVar Miner

Submissions for variant NM_004525.3(LRP2):c.1975+19G>A

dbSNP: rs2105443566
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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 RCV002216928 SCV002367572 likely benign not provided 2022-12-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494119 SCV002798767 likely benign Donnai-Barrow syndrome 2022-05-25 criteria provided, single submitter clinical testing

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