ClinVar Miner

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

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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000554.5(CRX):c.-116T>C	rs10418215	0.08435
NM_000554.6(CRX):c.*1900del	rs796977583
NM_000554.6(CRX):c.*308AAG[2]	rs398059782

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