ClinVar Miner

Submissions for variant NM_030930.4(UNC93B1):c.1724C>A (p.Pro575His)

gnomAD frequency: 0.00599  dbSNP: rs535779712
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 RCV000964210 SCV001111403 likely benign Herpes simplex encephalitis, susceptibility to, 1 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003396563 SCV004137049 benign not provided 2023-04-01 criteria provided, single submitter clinical testing UNC93B1: BS1, BS2

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