List of variants in gene CNGB1 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001297.5(CNGB1):c.-47A>G	rs186471030	0.00462
NM_001297.5(CNGB1):c.1626C>T (p.Thr542=)	rs148735841	0.00304
NM_001297.5(CNGB1):c.2958C>T (p.Asn986=)	rs543509332	0.00006
NM_001297.5(CNGB1):c.2853C>A (p.Asp951Glu)	rs7190978

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