ClinVar Miner

List of variants in gene RTN4IP1 reported as benign for Optic atrophy 10 with or without ataxia, intellectual disability, and seizures

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_032730.5(RTN4IP1):c.114T>A (p.Pro38=)	rs1987623	0.39946
NM_032730.5(RTN4IP1):c.495+27A>G	rs1870867	0.36066

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