List of variants in gene PDE6C reported as uncertain significance by Molecular Genetics Laboratory, Institute for Ophthalmic Research

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_006204.4(PDE6C):c.2156T>C (p.Met719Thr)	rs1460255181	0.00003
NM_006204.4(PDE6C):c.1637C>A (p.Thr546Asn)	rs143394832
NM_006204.4(PDE6C):c.2141T>A (p.Ile714Asn)	rs1064797148
NM_006204.4(PDE6C):c.2246G>A (p.Gly749Glu)	rs1554892155
NM_006204.4(PDE6C):c.2288T>C (p.Met763Thr)	rs1554892197
NM_006204.4(PDE6C):c.2294A>G (p.Asp765Gly)	rs1554892199
NM_006204.4(PDE6C):c.304C>T (p.Arg102Trp)	rs375795507

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