ClinVar Miner

Submissions for variant NM_030930.4(UNC93B1):c.1155C>T (p.Gly385=)

gnomAD frequency: 0.00844  dbSNP: rs200930438
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 RCV000531264 SCV000648200 benign Herpes simplex encephalitis, susceptibility to, 1 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718728 SCV005319189 benign not provided criteria provided, single submitter not provided

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