ClinVar Miner

Submissions for variant NM_030930.4(UNC93B1):c.239-6C>T

gnomAD frequency: 0.00183  dbSNP: rs182093266
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000647035 SCV000768822 benign Herpes simplex encephalitis, susceptibility to, 1 2025-02-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001702704 SCV004137057 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing UNC93B1: BP4
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702704 SCV001927320 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001702704 SCV001969018 likely benign not provided no assertion criteria provided clinical testing

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