ClinVar Miner

List of variants reported as benign for Leber congenital amaurosis 1 by Genome-Nilou Lab

Included ClinVar conditions (8):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000180.4(GUCY2D):c.2345T>A (p.Leu782His)	rs8069344	0.20071
NM_000180.4(GUCY2D):c.2576+37G>T	rs12103471	0.12387

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