List of variants in gene CRX reported as pathogenic for Leber congenital amaurosis 1

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_000554.6(CRX):c.443del (p.Gly148fs)	rs1968165374
NM_000554.6(CRX):c.500_501del (p.Ala166_Ser167insTer)	rs1599991611
NM_000554.6(CRX):c.[101-1G>A];[122G>A]

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