ClinVar Miner

Submissions for variant NM_152594.3(SPRED1):c.*578AT[13]

dbSNP: rs147547509
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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 RCV000268080 SCV000390805 uncertain significance Legius syndrome 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002292522 SCV002585486 benign not provided 2022-08-01 criteria provided, single submitter clinical testing SPRED1: BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV002292522 SCV005193699 uncertain significance not provided criteria provided, single submitter not provided

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