ClinVar Miner

Submissions for variant NM_015139.3(SLC35D1):c.393-5dup

dbSNP: rs5774854
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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 RCV002152226 SCV002416395 benign Schneckenbecken dysplasia 2023-07-27 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV002152226 SCV004563956 likely benign Schneckenbecken dysplasia 2023-10-19 criteria provided, single submitter clinical testing

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