ClinVar Miner

Submissions for variant NM_001371986.1(UNC80):c.3357+12A>G

gnomAD frequency: 0.00006  dbSNP: rs1164061431
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001864913 SCV002126812 likely benign not provided 2024-02-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001864913 SCV005188246 uncertain significance not provided criteria provided, single submitter not provided

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