ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.1958C>T (p.Thr653Ile)

dbSNP: rs121434503
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000008869 SCV000029079 risk factor Familial acute necrotizing encephalopathy 2009-01-01 no assertion criteria provided literature only
GeneReviews RCV000008869 SCV000212036 not provided Familial acute necrotizing encephalopathy no assertion provided literature only

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