List of variants in gene CNGB3 reported as benign for ABCA4-related retinopathy

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_019098.5(CNGB3):c.702T>G (p.Cys234Trp)	rs6471482	0.88912
NM_019098.5(CNGB3):c.892A>C (p.Thr298Pro)	rs4961206	0.64246
NM_019098.4(CNGB3):c.*1639C>A	rs990192	0.58635
NM_019098.4(CNGB3):c.*1638G>A	rs28471019	0.09910
NM_019098.5(CNGB3):c.2264A>G (p.Glu755Gly)	rs3735972	0.08238
NM_019098.5(CNGB3):c.2214A>G (p.Glu738=)	rs3735970	0.08236
NM_019098.5(CNGB3):c.919A>G (p.Ile307Val)	rs13265557	0.05793
NM_019098.5(CNGB3):c.1356G>A (p.Gln452=)	rs34839859	0.05572
NM_019098.5(CNGB3):c.608G>A (p.Arg203Gln)	rs16916632	0.05057
NM_019098.5(CNGB3):c.211+13T>G	rs66881636	0.04923
NM_019098.5(CNGB3):c.1781+10A>T	rs7000747	0.04709
NM_019098.5(CNGB3):c.*778T>C	rs16915859	0.01801
NM_019098.5(CNGB3):c.*389A>C	rs16915861	0.01797
NM_019098.5(CNGB3):c.354G>T (p.Pro118=)	rs75858066	0.01037
NM_019098.5(CNGB3):c.1397T>C (p.Met466Thr)	rs35010099	0.00978
NM_019098.5(CNGB3):c.494-11T>C	rs543970676	0.00078
NM_019098.4(CNGB3):c.-36T>G	rs7812496
NM_019098.5(CNGB3):c.*1303G>A	rs17683284
NM_019098.5(CNGB3):c.*735A>G	rs73269601
NM_019098.5(CNGB3):c.*915G>C	rs189446254

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