List of variants in gene XYLT2 reported as likely pathogenic for inherited vitreoretinopathy

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_022167.4(XYLT2):c.2548G>A (p.Asp850Asn)	rs1423415130	0.00001
NM_022167.4(XYLT2):c.1552del (p.Leu518fs)	rs1912543391
NM_022167.4(XYLT2):c.1584del (p.Gly529fs)
NM_022167.4(XYLT2):c.1584dup (p.Gly529fs)	rs779864368
NM_022167.4(XYLT2):c.1736del (p.Pro579fs)

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