ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.5871A>G (p.Glu1957=)

gnomAD frequency: 0.00024  dbSNP: rs202117246
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000939027 SCV001084861 likely benign Familial acute necrotizing encephalopathy 2022-07-05 criteria provided, single submitter clinical testing

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