ClinVar Miner

Submissions for variant NM_030930.4(UNC93B1):c.183C>T (p.Leu61=)

gnomAD frequency: 0.00008  dbSNP: rs1365228419
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
Invitae RCV001506244 SCV001711163 likely benign Herpes simplex encephalitis, susceptibility to, 1 2023-12-16 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000537555 SCV002497142 likely benign not provided 2022-02-01 criteria provided, single submitter clinical testing

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