List of variants in gene PDE6C reported as likely 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006204.4(PDE6C):c.2096A>C (p.Glu699Ala)	rs12261131	0.02167
NM_006204.4(PDE6C):c.2208+14A>C	rs61701022	0.00810
NM_006204.4(PDE6C):c.*26A>G	rs112520932	0.00703
NM_006204.4(PDE6C):c.1755G>T (p.Lys585Asn)	rs45522236	0.00677
NM_006204.4(PDE6C):c.203C>T (p.Thr68Ile)	rs62642544	0.00670
NM_006204.4(PDE6C):c.724-15G>T	rs141403797	0.00596
NM_006204.4(PDE6C):c.1936-9A>G	rs182445749	0.00536
NM_006204.4(PDE6C):c.*209T>C	rs530054025	0.00006
NM_006204.4(PDE6C):c.2466G>A (p.Lys822=)	rs79487435
NM_006204.4(PDE6C):c.2466G>C (p.Lys822Asn)	rs79487435
NM_006204.4(PDE6C):c.252G>T (p.Leu84=)	rs1131978

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