List of variants in gene CNGB1 reported as benign for not specified

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001297.5(CNGB1):c.2635-10C>T	rs437920	0.77649
NM_001297.5(CNGB1):c.2218-12C>T	rs483053	0.49292
NM_001297.5(CNGB1):c.1122-15C>T	rs2303778	0.46316
NM_001297.5(CNGB1):c.3462+7T>C	rs11076207	0.37846
NM_001297.5(CNGB1):c.327C>T (p.Gly109=)	rs17821448	0.36508
NM_001297.5(CNGB1):c.1958-14A>C	rs3991715	0.30656
NM_001297.5(CNGB1):c.2233C>A (p.Leu745Ile)	rs10459809	0.14066
NM_001297.5(CNGB1):c.1644T>C (p.Asp548=)	rs2161703	0.12201
NM_001297.5(CNGB1):c.2732A>G (p.Lys911Arg)	rs2303785	0.08900
NM_001297.5(CNGB1):c.3556C>T (p.Pro1186Ser)	rs7190372	0.02335
NM_001297.5(CNGB1):c.712G>A (p.Gly238Ser)	rs61745888	0.01420
NM_001297.5(CNGB1):c.606A>G (p.Glu202=)	rs76788887	0.01379
NM_001297.5(CNGB1):c.1382C>T (p.Thr461Met)	rs147593839	0.00806
NM_001297.5(CNGB1):c.634A>T (p.Thr212Ser)	rs192628905	0.00486
NM_001297.5(CNGB1):c.1580C>T (p.Ala527Val)	rs78292723	0.00257
NM_001297.5(CNGB1):c.2475C>T (p.Tyr825=)	rs200934249	0.00180
NM_001297.5(CNGB1):c.1204G>A (p.Asp402Asn)	rs140907154	0.00157
NM_001297.5(CNGB1):c.2526C>T (p.Thr842=)	rs185729258	0.00076
NM_001297.5(CNGB1):c.3584C>G (p.Ser1195Cys)	rs201186180	0.00066
NM_001297.5(CNGB1):c.2370-9C>T	rs374373659	0.00055
NM_001297.5(CNGB1):c.412+8C>A	rs185727761	0.00030
NM_001297.5(CNGB1):c.838-4G>T	rs375539469	0.00022
NM_001297.5(CNGB1):c.1179C>T (p.Asp393=)	rs377042647	0.00014
NM_001297.5(CNGB1):c.1089GGA[6] (p.Glu371dup)	rs141566950
NM_001297.5(CNGB1):c.1275C>G (p.Ala425=)	rs376016716
NM_001297.5(CNGB1):c.2634+8G>A	rs369567117
NM_001297.5(CNGB1):c.2664C>A (p.Ala888=)	rs413562
NM_001297.5(CNGB1):c.2664C>G (p.Ala888=)	rs413562
NM_001297.5(CNGB1):c.299G>A (p.Arg100His)	rs13336595

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