List of variants in gene PDE6C reported as benign for color vision disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_006204.4(PDE6C):c.1270-7A>G	rs616522	0.73216
NM_006204.4(PDE6C):c.1935+10C>A	rs1409332	0.43098
NM_006204.4(PDE6C):c.808T>A (p.Ser270Thr)	rs701865	0.39072
NM_006204.4(PDE6C):c.1098G>A (p.Ala366=)	rs714550	0.36884
NM_006204.4(PDE6C):c.1380C>G (p.Thr460=)	rs3737228	0.23737
NM_006204.4(PDE6C):c.282C>T (p.Asp94=)	rs12781149	0.07060
NM_006204.4(PDE6C):c.1270-9C>T	rs11187564	0.05345
NM_006204.4(PDE6C):c.471T>G (p.Asp157Glu)	rs76999928	0.00210
NM_006204.4(PDE6C):c.2466G>A (p.Lys822=)	rs79487435
NM_006204.4(PDE6C):c.252G>A (p.Leu84=)	rs1131978

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