List of variants in gene RTN4IP1 reported as likely pathogenic for not provided

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_032730.5(RTN4IP1):c.495+1G>A	rs1025800148	0.00001
NM_032730.5(RTN4IP1):c.620+1G>C	rs1360314039	0.00001
NC_000006.11:g.(?_107067057)_(107070864_?)dup
NC_000006.11:g.(?_107067077)_(107069368_?)dup
NM_032730.5(RTN4IP1):c.426+1G>T	rs1776515103
NM_032730.5(RTN4IP1):c.427-1_430delinsTGGCC	rs2114680188
NM_032730.5(RTN4IP1):c.890A>G (p.Tyr297Cys)	rs749329916
NM_032730.5(RTN4IP1):c.991-2A>G	rs2114628933

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