List of variants in gene PDE6A reported as likely benign by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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_000440.3(PDE6A):c.1476A>C (p.Gln492His)	rs17711594	0.00665
NM_000440.3(PDE6A):c.498G>A (p.Val166=)	rs138274547	0.00092
NM_000440.3(PDE6A):c.1408-11G>A	rs201527437	0.00059
NM_000440.3(PDE6A):c.177A>G (p.Glu59=)	rs146550067	0.00050

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