ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.775C>G (p.Leu259Val)

dbSNP: rs1695576898
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001329551 SCV001521021 uncertain significance Familial acute necrotizing encephalopathy 2019-05-30 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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