ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.8671G>A (p.Gly2891Ser)

gnomAD frequency: 0.00037  dbSNP: rs376940698
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 RCV000646026 SCV000767782 benign Familial acute necrotizing encephalopathy 2023-08-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004708974 SCV005246517 benign not provided criteria provided, single submitter not provided

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