List of variants in gene CNGB1 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001297.5(CNGB1):c.3115G>A (p.Gly1039Arg)	rs148999583	0.00372
NM_001297.5(CNGB1):c.3147C>T (p.His1049=)	rs200581517	0.00275
NM_001297.5(CNGB1):c.159+14C>T	rs199591689	0.00255
NM_001297.5(CNGB1):c.232G>A (p.Ala78Thr)	rs201407276	0.00131
NM_001297.5(CNGB1):c.2526C>T (p.Thr842=)	rs185729258	0.00076
NM_001297.5(CNGB1):c.2370-9C>T	rs374373659	0.00055
NM_001297.5(CNGB1):c.595C>T (p.Arg199Cys)	rs199583058	0.00054
NM_001297.5(CNGB1):c.838-4G>T	rs375539469	0.00022
NM_001297.5(CNGB1):c.139G>A (p.Glu47Lys)	rs78149232	0.00018
NM_001297.5(CNGB1):c.458+7C>T	rs368819628	0.00016
NM_001297.5(CNGB1):c.3693G>A (p.Pro1231=)	rs756850659	0.00002
NM_001297.5(CNGB1):c.2844C>T (p.Leu948=)	rs376791249	0.00001
NM_001297.5(CNGB1):c.3033C>T (p.Gly1011=)	rs772877765	0.00001
NM_001297.5(CNGB1):c.1011C>T (p.Asn337=)
NM_001297.5(CNGB1):c.2094C>T (p.Cys698=)	rs563059002
NM_001297.5(CNGB1):c.2634+8G>A	rs369567117
NM_001297.5(CNGB1):c.270T>G (p.Ala90=)

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