List of variants in gene CNGB1 reported as 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001297.5(CNGB1):c.2635-10C>T	rs437920	0.77649
NM_001297.5(CNGB1):c.1958-14A>C	rs3991715	0.30656
NM_001297.5(CNGB1):c.376G>C (p.Ala126Pro)	rs200332871	0.00219
NM_001297.5(CNGB1):c.1435C>A (p.Leu479Ile)	rs2303783	0.00014
NM_001297.5(CNGB1):c.3309G>A (p.Ala1103=)	rs201319323	0.00004
NM_001297.5(CNGB1):c.3560G>A (p.Arg1187Gln)	rs543712958	0.00004
NM_001297.5(CNGB1):c.90G>A (p.Glu30=)	rs375219355	0.00002
NM_001297.5(CNGB1):c.2664C>G (p.Ala888=)	rs413562

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