ClinVar Miner

Submissions for variant NM_005045.4(RELN):c.-24GGC[7]

dbSNP: rs55656324
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000406489 SCV000466005 uncertain significance Lissencephaly, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001712347 SCV001945737 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001712347 SCV004042312 benign not provided 2023-09-01 criteria provided, single submitter clinical testing RELN: BP4, BS1, BS2

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