List of variants in gene CNGB3 reported as benign by Eurofins NTD LLC (GA)

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_019098.5(CNGB3):c.892A>C (p.Thr298Pro)	rs4961206	0.64246
NM_019098.5(CNGB3):c.2264A>G (p.Glu755Gly)	rs3735972	0.08214
NM_019098.5(CNGB3):c.2214A>G (p.Glu738=)	rs3735970	0.08211
NM_019098.5(CNGB3):c.2415A>C (p.Glu805Asp)	rs186448979	0.00025

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