List of variants in gene GNAT2 reported as benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001377295.2(GNAT2):c.546G>A (p.Thr182=)	rs1799875	0.35862
NM_001377295.2(GNAT2):c.-32A>G	rs2304355	0.12857
NM_001377295.2(GNAT2):c.319C>A (p.Leu107Ile)	rs3738766	0.02487
NM_001377295.2(GNAT2):c.369C>T (p.Leu123=)	rs12046787	0.00028

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