ClinVar Miner

List of variants reported as benign for Leber congenital amaurosis 1 by Fulgent Genetics, Fulgent Genetics

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.154G>T (p.Ala52Ser)	rs61749665	0.29501
NM_000180.4(GUCY2D):c.2101C>T (p.Pro701Ser)	rs34598902	0.03505

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