List of variants in gene CNGB3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_019098.5(CNGB3):c.853-45T>C	rs75861378	0.01223
NM_019098.5(CNGB3):c.354G>T (p.Pro118=)	rs75858066	0.01037
NM_019098.5(CNGB3):c.2415A>C (p.Glu805Asp)	rs186448979	0.00025
NM_019098.5(CNGB3):c.12G>A (p.Ser4=)	rs139284415	0.00015
NM_019098.5(CNGB3):c.503C>T (p.Thr168Met)	rs755130011	0.00009
NM_019098.5(CNGB3):c.339-10dup	rs200792506

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