ClinVar Miner

Submissions for variant NM_032730.5(RTN4IP1):c.495+27A>G

gnomAD frequency: 0.36066  dbSNP: rs1870867
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001651442 SCV001864317 benign not provided 2021-05-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796639 SCV002032863 benign Optic atrophy 10 with or without ataxia, intellectual disability, and seizures 2021-11-07 criteria provided, single submitter clinical testing

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