List of variants in gene combination GNAT2, LOC129388577 reported as uncertain significance for color vision disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001377295.2(GNAT2):c.609G>T (p.Gly203=)	rs551776784	0.00008
NM_001377295.2(GNAT2):c.672T>C (p.Cys224=)	rs201230566	0.00001
NM_001377295.2(GNAT2):c.715G>A (p.Glu239Lys)	rs140788789	0.00001
NM_001377295.2(GNAT2):c.620A>T (p.Glu207Val)	rs1557918619
NM_001377295.2(GNAT2):c.623G>C (p.Arg208Thr)	rs995152260

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