ClinVar Miner

Submissions for variant NM_003383.5(VLDLR):c.943+10del

dbSNP: rs761373572
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000291026 SCV000479345 uncertain significance Congenital cerebellar hypoplasia 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058794 SCV002451510 benign not provided 2024-03-08 criteria provided, single submitter clinical testing

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