List of variants in gene KIAA1549 reported as likely pathogenic for retinal disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001164665.2(KIAA1549):c.1796_1797del (p.Glu599fs)
NM_001164665.2(KIAA1549):c.2132C>T (p.Pro711Leu)
NM_001164665.2(KIAA1549):c.4519C>T (p.Arg1507Ter)

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