ClinVar Miner

List of variants in gene CNGB3 reported as likely benign for Stargardt Disease, Recessive

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_019098.5(CNGB3):c.909_910del	rs3217489	0.08432
NM_019098.5(CNGB3):c.494-11dup	rs36008065

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