List of variants in gene RTN4IP1 reported as pathogenic for optic atrophy

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)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_032730.5(RTN4IP1):c.308G>A (p.Arg103His)	rs372054380	0.00003
NM_032730.5(RTN4IP1):c.601A>T (p.Lys201Ter)	rs200457692	0.00001
NM_032730.5(RTN4IP1):c.806+1G>A	rs772984484	0.00001
NM_032730.5(RTN4IP1):c.2T>C (p.Met1Thr)	rs2114691078
NM_032730.5(RTN4IP1):c.432G>A (p.Trp144Ter)	rs755175825
NM_032730.5(RTN4IP1):c.500C>T (p.Ser167Phe)	rs2114677062
NM_032730.5(RTN4IP1):c.962G>A (p.Gly321Glu)	rs145695118

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